Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
8,177
archived clinical trials in
Orthopedic

Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Montana Neuro Science Institute; St. Patrick's Medical Center
mi
from
Missoula, MT
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Montana Neuro Science Institute; St. Patrick's Medical Center
mi
from
Missoula, MT
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
University at Buffalo Neurosurgery, Inc. Kaleida Health-Buffalo General Medical center/Gates Vascular Institute
mi
from
Buffalo, NY
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
University at Buffalo Neurosurgery, Inc. Kaleida Health-Buffalo General Medical center/Gates Vascular Institute
mi
from
Buffalo, NY
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Buffalo Neurosurgery Group
mi
from
West Seneca, NY
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Buffalo Neurosurgery Group
mi
from
West Seneca, NY
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Crystal Clinic, Inc.; Akron General Medical Center
mi
from
Akron, OH
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Crystal Clinic, Inc.; Akron General Medical Center
mi
from
Akron, OH
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Central Ohio Neurological Surgeons; Mt. Carmel East Hospital
mi
from
Westerville, OH
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Central Ohio Neurological Surgeons; Mt. Carmel East Hospital
mi
from
Westerville, OH
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
The Center Orthopaedic & Neurosurgical Care & Research
mi
from
Bend, OR
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
The Center Orthopaedic & Neurosurgical Care & Research
mi
from
Bend, OR
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
OAA Orthopaedic Specialists
mi
from
Allentown, PA
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
OAA Orthopaedic Specialists
mi
from
Allentown, PA
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Allegheny Neurosurgery; Washington Hospital
mi
from
Pittsburgh, PA
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Allegheny Neurosurgery; Washington Hospital
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Lexington Brain and Spine Institute
mi
from
West Columbia, SC
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Lexington Brain and Spine Institute
mi
from
West Columbia, SC
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Center for Sports Medicine and Orthopaedics; Memorial Hospital
mi
from
Chattanooga, TN
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Center for Sports Medicine and Orthopaedics; Memorial Hospital
mi
from
Chattanooga, TN
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
East Tennessee Brain & Spine Center, Johnson City Medical Center
mi
from
Johnson City, TN
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
East Tennessee Brain & Spine Center, Johnson City Medical Center
mi
from
Johnson City, TN
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Central Texas Spine Institute; Health South Surgical Center
mi
from
Austin, TX
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Central Texas Spine Institute; Health South Surgical Center
mi
from
Austin, TX
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Virginia Brain and Spine; Winchester Medical Center
mi
from
Winchester, VA
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Virginia Brain and Spine; Winchester Medical Center
mi
from
Winchester, VA
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
West Virginia University; Ruby Memorial Hospital, WVU Hospitals, Inc.
mi
from
Morgantown, WV
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
West Virginia University; Ruby Memorial Hospital, WVU Hospitals, Inc.
mi
from
Morgantown, WV
Click here to add this to my saved trials
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated:  4/3/2018
Henry Ford Hospital
mi
from
West Bloomfield, MI
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
A Prospective, Randomized, Controlled, Multicenter Pivotal Clinical Trial of the Artificial Cervical Disc-LP at Two Levels for Symptomatic Cervical Disc Disease
Status: Enrolling
Updated: 4/3/2018
Henry Ford Hospital
mi
from
West Bloomfield, MI
Click here to add this to my saved trials
Single Injection Adductor Canal Block Versus Continuous Adductor Canal Infusion for Total Knee Arthroplasty
Single Injection Adductor Canal Block Versus Continuous Adductor Canal Infusion for Total Knee Arthroplasty
Status: Enrolling
Updated:  4/3/2018
Wake Forest Baptist Hospital
mi
from
Winston-Salem, NC
Single Injection Adductor Canal Block Versus Continuous Adductor Canal Infusion for Total Knee Arthroplasty
Single Injection Adductor Canal Block Versus Continuous Adductor Canal Infusion for Total Knee Arthroplasty
Status: Enrolling
Updated: 4/3/2018
Wake Forest Baptist Hospital
mi
from
Winston-Salem, NC
Click here to add this to my saved trials
Efficacy of Peri-Incisional Multimodal Drug Injection Following Operative Management of Femur Fractures
Efficacy of Peri-Incisional Multimodal Drug Injection Following Operative Management of Femur Fractures: A Randomized Controlled Trial
Status: Enrolling
Updated:  4/3/2018
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
Efficacy of Peri-Incisional Multimodal Drug Injection Following Operative Management of Femur Fractures
Efficacy of Peri-Incisional Multimodal Drug Injection Following Operative Management of Femur Fractures: A Randomized Controlled Trial
Status: Enrolling
Updated: 4/3/2018
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
Click here to add this to my saved trials
Studies of Heritable Disorders of Connective Tissue
Clinical and Molecular Manifestations of Heritable Disorders of Connective Tissue
Status: Enrolling
Updated:  4/4/2018
National Institute of Aging, Clinical Research Unit
mi
from
Baltimore, MD
Studies of Heritable Disorders of Connective Tissue
Clinical and Molecular Manifestations of Heritable Disorders of Connective Tissue
Status: Enrolling
Updated: 4/4/2018
National Institute of Aging, Clinical Research Unit
mi
from
Baltimore, MD
Click here to add this to my saved trials
The PTC124 (Ataluren) Clinical Trial for Duchenne Muscular Dystrophy: Exploration of the Experiences of Parents, Clinician Researchers, and the Industry Sponsor
The PTC124 (Ataluren) Clinical Trial for Duchenne Muscular Dystrophy: Exploration of the Experiences of Parents, Clinician Researchers, and the Industry Sponsor
Status: Enrolling
Updated:  4/4/2018
National Human Genome Research Institute (NHGRI), 9000 Rockville Pike
mi
from
Bethesda, MD
The PTC124 (Ataluren) Clinical Trial for Duchenne Muscular Dystrophy: Exploration of the Experiences of Parents, Clinician Researchers, and the Industry Sponsor
The PTC124 (Ataluren) Clinical Trial for Duchenne Muscular Dystrophy: Exploration of the Experiences of Parents, Clinician Researchers, and the Industry Sponsor
Status: Enrolling
Updated: 4/4/2018
National Human Genome Research Institute (NHGRI), 9000 Rockville Pike
mi
from
Bethesda, MD
Click here to add this to my saved trials
Skeletal Muscle Inflammation, Oxidative Stress and DNA Repair in Age-Related Sarcopenia
Claude D. Pepper Older Americans Independence Center (OAIC); Skeletal Muscle Inflammation, Oxidative Stress and DNA Repair in Age-Related Sarcopenia
Status: Enrolling
Updated:  4/4/2018
University of Florida
mi
from
Gainesville, FL
Skeletal Muscle Inflammation, Oxidative Stress and DNA Repair in Age-Related Sarcopenia
Claude D. Pepper Older Americans Independence Center (OAIC); Skeletal Muscle Inflammation, Oxidative Stress and DNA Repair in Age-Related Sarcopenia
Status: Enrolling
Updated: 4/4/2018
University of Florida
mi
from
Gainesville, FL
Click here to add this to my saved trials
The Strong Brain Study
A Pilot Study to Evaluate the Role of Brain Integrity on Post-hospital Sarcopenia
Status: Enrolling
Updated:  4/4/2018
Institute on Aging
mi
from
Gainesville, FL
The Strong Brain Study
A Pilot Study to Evaluate the Role of Brain Integrity on Post-hospital Sarcopenia
Status: Enrolling
Updated: 4/4/2018
Institute on Aging
mi
from
Gainesville, FL
Click here to add this to my saved trials
Effects of IV-Administered Ca-DTPA and Zn-DTPA To Treat Patients With Gadolinium Deposition Disease
Investigator Initiated Investigational New Drug Application to Study the Effects of IV-Administered Ca-DTPA and Zn-DTPA To Treat Patients With Gadolinium Deposition Disease
Status: Enrolling
Updated:  4/5/2018
UNC Hospitals
mi
from
Chapel Hill, NC
Effects of IV-Administered Ca-DTPA and Zn-DTPA To Treat Patients With Gadolinium Deposition Disease
Investigator Initiated Investigational New Drug Application to Study the Effects of IV-Administered Ca-DTPA and Zn-DTPA To Treat Patients With Gadolinium Deposition Disease
Status: Enrolling
Updated: 4/5/2018
UNC Hospitals
mi
from
Chapel Hill, NC
Click here to add this to my saved trials
Percutaneous US Guided Elbow Tenotomy With the TenJet HydroSurgery System
Prospective Multi-Center Evaluation of Percutaneous Ultrasound Guided Elbow Tenotomy (PUGET) Using the HydroCision TenJet HydroSurgery System
Status: Enrolling
Updated:  4/6/2018
Orthopaedic Associates of Muskegon
mi
from
Muskegon, MI
Percutaneous US Guided Elbow Tenotomy With the TenJet HydroSurgery System
Prospective Multi-Center Evaluation of Percutaneous Ultrasound Guided Elbow Tenotomy (PUGET) Using the HydroCision TenJet HydroSurgery System
Status: Enrolling
Updated: 4/6/2018
Orthopaedic Associates of Muskegon
mi
from
Muskegon, MI
Click here to add this to my saved trials
Percutaneous US Guided Elbow Tenotomy With the TenJet HydroSurgery System
Prospective Multi-Center Evaluation of Percutaneous Ultrasound Guided Elbow Tenotomy (PUGET) Using the HydroCision TenJet HydroSurgery System
Status: Enrolling
Updated:  4/6/2018
Penn Highlands
mi
from
DuBois, PA
Percutaneous US Guided Elbow Tenotomy With the TenJet HydroSurgery System
Prospective Multi-Center Evaluation of Percutaneous Ultrasound Guided Elbow Tenotomy (PUGET) Using the HydroCision TenJet HydroSurgery System
Status: Enrolling
Updated: 4/6/2018
Penn Highlands
mi
from
DuBois, PA
Click here to add this to my saved trials
Percutaneous US Guided Elbow Tenotomy With the TenJet HydroSurgery System
Prospective Multi-Center Evaluation of Percutaneous Ultrasound Guided Elbow Tenotomy (PUGET) Using the HydroCision TenJet HydroSurgery System
Status: Enrolling
Updated:  4/6/2018
Noble Pain Management & Sports Medicine
mi
from
Fort Worth, TX
Percutaneous US Guided Elbow Tenotomy With the TenJet HydroSurgery System
Prospective Multi-Center Evaluation of Percutaneous Ultrasound Guided Elbow Tenotomy (PUGET) Using the HydroCision TenJet HydroSurgery System
Status: Enrolling
Updated: 4/6/2018
Noble Pain Management & Sports Medicine
mi
from
Fort Worth, TX
Click here to add this to my saved trials
Maintenance of Shoulder Health and Function After Spinal Cord Injury
Southern California Spinal Cord Injury Model System: A Randomized Clinical Trial to Evaluate Two Prevention Programs for Maintenance of Shoulder Health and Function After Spinal Cord Injury
Status: Enrolling
Updated:  4/9/2018
Rancho Los Amigos National Rehabilitaiton Center
mi
from
Downey, CA
Maintenance of Shoulder Health and Function After Spinal Cord Injury
Southern California Spinal Cord Injury Model System: A Randomized Clinical Trial to Evaluate Two Prevention Programs for Maintenance of Shoulder Health and Function After Spinal Cord Injury
Status: Enrolling
Updated: 4/9/2018
Rancho Los Amigos National Rehabilitaiton Center
mi
from
Downey, CA
Click here to add this to my saved trials
Psychological Concomitants of Morquio A Syndrome - Longitudinal Effects of Enzyme Replacement Therapy (The MAPLE Study)
Psychological Concomitants of Morquio A Syndrome - Longitudinal Effects of Enzyme Replacement Therapy
Status: Enrolling
Updated:  4/9/2018
Emory University
mi
from
Decatur, GA
Psychological Concomitants of Morquio A Syndrome - Longitudinal Effects of Enzyme Replacement Therapy (The MAPLE Study)
Psychological Concomitants of Morquio A Syndrome - Longitudinal Effects of Enzyme Replacement Therapy
Status: Enrolling
Updated: 4/9/2018
Emory University
mi
from
Decatur, GA
Click here to add this to my saved trials
PK Study of EXPAREL in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
A Phase 1, Open-Label Study to Evaluate the Safety and Pharmacokinetics of Local Administration of EXPAREL When Administered for Prolonged Postsurgical Analgesia in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
Status: Enrolling
Updated:  4/9/2018
University of Miami
mi
from
Miami, FL
PK Study of EXPAREL in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
A Phase 1, Open-Label Study to Evaluate the Safety and Pharmacokinetics of Local Administration of EXPAREL When Administered for Prolonged Postsurgical Analgesia in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
Status: Enrolling
Updated: 4/9/2018
University of Miami
mi
from
Miami, FL
Click here to add this to my saved trials
PK Study of EXPAREL in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
A Phase 1, Open-Label Study to Evaluate the Safety and Pharmacokinetics of Local Administration of EXPAREL When Administered for Prolonged Postsurgical Analgesia in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
Status: Enrolling
Updated:  4/9/2018
The Ohio State University, Wexner Medical Center
mi
from
Columbus, OH
PK Study of EXPAREL in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
A Phase 1, Open-Label Study to Evaluate the Safety and Pharmacokinetics of Local Administration of EXPAREL When Administered for Prolonged Postsurgical Analgesia in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
Status: Enrolling
Updated: 4/9/2018
The Ohio State University, Wexner Medical Center
mi
from
Columbus, OH
Click here to add this to my saved trials
PK Study of EXPAREL in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
A Phase 1, Open-Label Study to Evaluate the Safety and Pharmacokinetics of Local Administration of EXPAREL When Administered for Prolonged Postsurgical Analgesia in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
Status: Enrolling
Updated:  4/9/2018
Thomas Jefferson University
mi
from
Philadelphia, PA
PK Study of EXPAREL in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
A Phase 1, Open-Label Study to Evaluate the Safety and Pharmacokinetics of Local Administration of EXPAREL When Administered for Prolonged Postsurgical Analgesia in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery
Status: Enrolling
Updated: 4/9/2018
Thomas Jefferson University
mi
from
Philadelphia, PA
Click here to add this to my saved trials
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated:  4/10/2018
Orthopedic Research Institute
mi
from
Boynton Beach, FL
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated: 4/10/2018
Orthopedic Research Institute
mi
from
Boynton Beach, FL
Click here to add this to my saved trials
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated:  4/10/2018
Infinite Clinical Research
mi
from
Doral, FL
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated: 4/10/2018
Infinite Clinical Research
mi
from
Doral, FL
Click here to add this to my saved trials
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated:  4/10/2018
Shrock Orthopedic Research, LLC
mi
from
Fort Lauderdale, FL
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated: 4/10/2018
Shrock Orthopedic Research, LLC
mi
from
Fort Lauderdale, FL
Click here to add this to my saved trials
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated:  4/10/2018
Center for Advanced Research & Education
mi
from
Gainesville, GA
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated: 4/10/2018
Center for Advanced Research & Education
mi
from
Gainesville, GA
Click here to add this to my saved trials
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated:  4/10/2018
Orthopaedic Association of Michigan
mi
from
Grand Rapids, MI
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated: 4/10/2018
Orthopaedic Association of Michigan
mi
from
Grand Rapids, MI
Click here to add this to my saved trials
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated:  4/10/2018
University of Wisconsin Osteoporosis Clinical and Research Program
mi
from
Madison, WI
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated: 4/10/2018
University of Wisconsin Osteoporosis Clinical and Research Program
mi
from
Madison, WI
Click here to add this to my saved trials
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated:  4/10/2018
Duurga Clinical Service
mi
from
Yorba Linda, CA
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated: 4/10/2018
Duurga Clinical Service
mi
from
Yorba Linda, CA
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Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated:  4/10/2018
Szent János Kórház és Észak budai Egyesített Kórházak Traumatológiai és Kézsebészeti Osztály
mi
from
Budapest,
Acute Hip Fracture Study in Patients 65 Years or Greater
A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects With Acute Hip Fracture
Status: Enrolling
Updated: 4/10/2018
Szent János Kórház és Észak budai Egyesített Kórházak Traumatológiai és Kézsebészeti Osztály
mi
from
Budapest,
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Efficacy and Safety of Valsartan and Nebivolol/Valsartan in Hypertensive Patients With LVH
A Prospective, Randomized, Open-Label, 13 to 14-week Study of the Efficacy and Safety of Valsartan and Nebivolol/Valsartan in Hypertensive Subjects With Left Ventricular Hypertrophy (LVH)
Status: Enrolling
Updated:  4/10/2018
Trinity Hypertension & Metabolic Research Institute
mi
from
Carrollton, TX
Efficacy and Safety of Valsartan and Nebivolol/Valsartan in Hypertensive Patients With LVH
A Prospective, Randomized, Open-Label, 13 to 14-week Study of the Efficacy and Safety of Valsartan and Nebivolol/Valsartan in Hypertensive Subjects With Left Ventricular Hypertrophy (LVH)
Status: Enrolling
Updated: 4/10/2018
Trinity Hypertension & Metabolic Research Institute
mi
from
Carrollton, TX
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Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Status: Enrolling
Updated:  4/11/2018
Campbell Clinic
mi
from
Germantown, TN
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Status: Enrolling
Updated: 4/11/2018
Campbell Clinic
mi
from
Germantown, TN
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Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Status: Enrolling
Updated:  4/11/2018
Institute for Foot and Ankle Reconstruction at Mercy
mi
from
Baltimore, MD
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Status: Enrolling
Updated: 4/11/2018
Institute for Foot and Ankle Reconstruction at Mercy
mi
from
Baltimore, MD
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Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Status: Enrolling
Updated:  4/11/2018
Minnesota Orthopedic Sports Medicine Institute (MOSMI)
mi
from
Edina, MN
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Status: Enrolling
Updated: 4/11/2018
Minnesota Orthopedic Sports Medicine Institute (MOSMI)
mi
from
Edina, MN
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Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Status: Enrolling
Updated:  4/11/2018
Orthopaedic Associates of Michigan
mi
from
Grand Rapids, MI
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Status: Enrolling
Updated: 4/11/2018
Orthopaedic Associates of Michigan
mi
from
Grand Rapids, MI
Click here to add this to my saved trials
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Status: Enrolling
Updated:  4/11/2018
Penn State Milton S. Hershey Medical Center
mi
from
Hershey, PA
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft
Status: Enrolling
Updated: 4/11/2018
Penn State Milton S. Hershey Medical Center
mi
from
Hershey, PA
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Testosterone in Treating Postmenopausal Patients With Arthralgia Caused by Adjuvant Aromatase Inhibitor Treatment
Randomized Double-Blind Placebo Controlled Study of Testosterone in the Adjuvant Treatment of Postmenopausal Women With Aromatase Inhibitor Induced Arthralgias
Status: Enrolling
Updated:  4/12/2018
Sutter Auburn Faith Hospital
mi
from
Auburn, CA
Testosterone in Treating Postmenopausal Patients With Arthralgia Caused by Adjuvant Aromatase Inhibitor Treatment
Randomized Double-Blind Placebo Controlled Study of Testosterone in the Adjuvant Treatment of Postmenopausal Women With Aromatase Inhibitor Induced Arthralgias
Status: Enrolling
Updated: 4/12/2018
Sutter Auburn Faith Hospital
mi
from
Auburn, CA
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Testosterone in Treating Postmenopausal Patients With Arthralgia Caused by Adjuvant Aromatase Inhibitor Treatment
Randomized Double-Blind Placebo Controlled Study of Testosterone in the Adjuvant Treatment of Postmenopausal Women With Aromatase Inhibitor Induced Arthralgias
Status: Enrolling
Updated:  4/12/2018
Sutter Cancer Centers Radiation Oncology Services-Auburn
mi
from
Auburn, CA
Testosterone in Treating Postmenopausal Patients With Arthralgia Caused by Adjuvant Aromatase Inhibitor Treatment
Randomized Double-Blind Placebo Controlled Study of Testosterone in the Adjuvant Treatment of Postmenopausal Women With Aromatase Inhibitor Induced Arthralgias
Status: Enrolling
Updated: 4/12/2018
Sutter Cancer Centers Radiation Oncology Services-Auburn
mi
from
Auburn, CA
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Testosterone in Treating Postmenopausal Patients With Arthralgia Caused by Adjuvant Aromatase Inhibitor Treatment
Randomized Double-Blind Placebo Controlled Study of Testosterone in the Adjuvant Treatment of Postmenopausal Women With Aromatase Inhibitor Induced Arthralgias
Status: Enrolling
Updated:  4/12/2018
Alta Bates Summit Medical Center-Herrick Campus
mi
from
Berkeley, CA
Testosterone in Treating Postmenopausal Patients With Arthralgia Caused by Adjuvant Aromatase Inhibitor Treatment
Randomized Double-Blind Placebo Controlled Study of Testosterone in the Adjuvant Treatment of Postmenopausal Women With Aromatase Inhibitor Induced Arthralgias
Status: Enrolling
Updated: 4/12/2018
Alta Bates Summit Medical Center-Herrick Campus
mi
from
Berkeley, CA
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Testosterone in Treating Postmenopausal Patients With Arthralgia Caused by Adjuvant Aromatase Inhibitor Treatment
Randomized Double-Blind Placebo Controlled Study of Testosterone in the Adjuvant Treatment of Postmenopausal Women With Aromatase Inhibitor Induced Arthralgias
Status: Enrolling
Updated:  4/12/2018
Sutter Cancer Centers Radiation Oncology Services-Cameron Park
mi
from
Cameron Park, CA
Testosterone in Treating Postmenopausal Patients With Arthralgia Caused by Adjuvant Aromatase Inhibitor Treatment
Randomized Double-Blind Placebo Controlled Study of Testosterone in the Adjuvant Treatment of Postmenopausal Women With Aromatase Inhibitor Induced Arthralgias
Status: Enrolling
Updated: 4/12/2018
Sutter Cancer Centers Radiation Oncology Services-Cameron Park
mi
from
Cameron Park, CA
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Testosterone in Treating Postmenopausal Patients With Arthralgia Caused by Adjuvant Aromatase Inhibitor Treatment
Randomized Double-Blind Placebo Controlled Study of Testosterone in the Adjuvant Treatment of Postmenopausal Women With Aromatase Inhibitor Induced Arthralgias
Status: Enrolling
Updated:  4/12/2018
Eden Hospital Medical Center
mi
from
Castro Valley, CA
Testosterone in Treating Postmenopausal Patients With Arthralgia Caused by Adjuvant Aromatase Inhibitor Treatment
Randomized Double-Blind Placebo Controlled Study of Testosterone in the Adjuvant Treatment of Postmenopausal Women With Aromatase Inhibitor Induced Arthralgias
Status: Enrolling
Updated: 4/12/2018
Eden Hospital Medical Center
mi
from
Castro Valley, CA
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Testosterone in Treating Postmenopausal Patients With Arthralgia Caused by Adjuvant Aromatase Inhibitor Treatment
Randomized Double-Blind Placebo Controlled Study of Testosterone in the Adjuvant Treatment of Postmenopausal Women With Aromatase Inhibitor Induced Arthralgias
Status: Enrolling
Updated:  4/12/2018
Sutter Davis Hospital
mi
from
Davis, CA
Testosterone in Treating Postmenopausal Patients With Arthralgia Caused by Adjuvant Aromatase Inhibitor Treatment
Randomized Double-Blind Placebo Controlled Study of Testosterone in the Adjuvant Treatment of Postmenopausal Women With Aromatase Inhibitor Induced Arthralgias
Status: Enrolling
Updated: 4/12/2018
Sutter Davis Hospital
mi
from
Davis, CA
Click here to add this to my saved trials