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

Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
Rush University Medical Center
mi
from
Chicago, IL
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
Rush University Medical Center
mi
from
Chicago, IL
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
University of Illinois at Chicago
mi
from
Chicago, IL
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
University of Illinois at Chicago
mi
from
Chicago, IL
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
University of Kansas Medical Center
mi
from
Kansas City, KA
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
University of Kansas Medical Center
mi
from
Kansas City, KA
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
Willis Knighton River Cities Clinical Research Center
mi
from
Shreveport, LA
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
Willis Knighton River Cities Clinical Research Center
mi
from
Shreveport, LA
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
Comprehensive Pain & Rehabilitation
mi
from
Pascagoula, MS
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
Comprehensive Pain & Rehabilitation
mi
from
Pascagoula, MS
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
Mercy Medical Research Institute
mi
from
Springfield, MO
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
Mercy Medical Research Institute
mi
from
Springfield, MO
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
NYU Langone Medical Center
mi
from
New York City, NY
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
NYU Langone Medical Center
mi
from
New York City, NY
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
Mayfield Clinic
mi
from
Cincinnati, OH
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
Mayfield Clinic
mi
from
Cincinnati, OH
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
University Hospitals at Case Medical Center
mi
from
Cleveland, OH
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
University Hospitals at Case Medical Center
mi
from
Cleveland, OH
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
Thomas Jefferson University
mi
from
Philadelphia, PA
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
Thomas Jefferson University
mi
from
Philadelphia, PA
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
Southern Spine Institute
mi
from
Mount Pleasant, SC
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
Southern Spine Institute
mi
from
Mount Pleasant, SC
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
Austin Pain Associates
mi
from
Austin, TX
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
Austin Pain Associates
mi
from
Austin, TX
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
Space City Pain Specialists
mi
from
Webster, TX
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
Space City Pain Specialists
mi
from
Webster, TX
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
Lifetree Clinical Research
mi
from
Salt Lake City, UT
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
Lifetree Clinical Research
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated:  3/24/2016
Wisconsin Health Center Surgery Center
mi
from
Greenfield, WI
Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients
SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666
Status: Enrolling
Updated: 3/24/2016
Wisconsin Health Center Surgery Center
mi
from
Greenfield, WI
Click here to add this to my saved trials
Study of the Effect of a Calcium-rich Diet on Bone Health in Girls
Effect of Calcium Foods on Bone Quality in Pubertal Females
Status: Enrolling
Updated:  3/24/2016
Creighton University
mi
from
Omaha, NE
Study of the Effect of a Calcium-rich Diet on Bone Health in Girls
Effect of Calcium Foods on Bone Quality in Pubertal Females
Status: Enrolling
Updated: 3/24/2016
Creighton University
mi
from
Omaha, NE
Click here to add this to my saved trials
Improving Muscle Assessment in Older Adults - The "Can We Build a Better Mouse Trap?" Study
Improving Muscle Assessment in Older Adults - The "Can We Build a Better Mouse Trap?" Study
Status: Enrolling
Updated:  3/25/2016
University of Wisconsin-Madison Osteoporosis Clinical Research Program
mi
from
Madison, WI
Improving Muscle Assessment in Older Adults - The "Can We Build a Better Mouse Trap?" Study
Improving Muscle Assessment in Older Adults - The "Can We Build a Better Mouse Trap?" Study
Status: Enrolling
Updated: 3/25/2016
University of Wisconsin-Madison Osteoporosis Clinical Research Program
mi
from
Madison, WI
Click here to add this to my saved trials
PurTox (Botulinum Toxin Type A) for the Treatment of Adult Onset Spasmodic Torticollis/Cervical Dystonia
A Phase I, Single-dose, Double-blind, Placebo Controlled, Dose Escalation Study to Evaluate the Safety of PurTox for the Treatment of Adult Onset Spasmodic Torticollis/Cervical Dystonia and to Explore Dose-associated Efficacy
Status: Enrolling
Updated:  3/25/2016
Mentor Worldwide LLC
mi
from
Santa Barbara, CA
PurTox (Botulinum Toxin Type A) for the Treatment of Adult Onset Spasmodic Torticollis/Cervical Dystonia
A Phase I, Single-dose, Double-blind, Placebo Controlled, Dose Escalation Study to Evaluate the Safety of PurTox for the Treatment of Adult Onset Spasmodic Torticollis/Cervical Dystonia and to Explore Dose-associated Efficacy
Status: Enrolling
Updated: 3/25/2016
Mentor Worldwide LLC
mi
from
Santa Barbara, CA
Click here to add this to my saved trials
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated:  3/28/2016
St. Helena Hospital
mi
from
St. Helena, CA
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated: 3/28/2016
St. Helena Hospital
mi
from
St. Helena, CA
Click here to add this to my saved trials
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated:  3/28/2016
Holy Cross Orthopedic Institute
mi
from
Fort Lauderdale, FL
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated: 3/28/2016
Holy Cross Orthopedic Institute
mi
from
Fort Lauderdale, FL
Click here to add this to my saved trials
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated:  3/28/2016
Naples Community Hospital
mi
from
Naples, FL
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated: 3/28/2016
Naples Community Hospital
mi
from
Naples, FL
Click here to add this to my saved trials
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated:  3/28/2016
Tampa General/FORE
mi
from
Tampa, FL
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated: 3/28/2016
Tampa General/FORE
mi
from
Tampa, FL
Click here to add this to my saved trials
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated:  3/28/2016
Emory Healthcare - St. Joseph's Research Institute
mi
from
Atlanta, GA
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated: 3/28/2016
Emory Healthcare - St. Joseph's Research Institute
mi
from
Atlanta, GA
Click here to add this to my saved trials
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated:  3/28/2016
Spectrum Health/Orthopaedic Associates of Michigan
mi
from
Grand Rapids, MI
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated: 3/28/2016
Spectrum Health/Orthopaedic Associates of Michigan
mi
from
Grand Rapids, MI
Click here to add this to my saved trials
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated:  3/28/2016
Trinity Health/Bone and Joint Institute
mi
from
Port Huron, MI
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated: 3/28/2016
Trinity Health/Bone and Joint Institute
mi
from
Port Huron, MI
Click here to add this to my saved trials
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated:  3/28/2016
University of Wisconsin
mi
from
Madison, WI
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the VERASENSE™ Knee System
Status: Enrolling
Updated: 3/28/2016
University of Wisconsin
mi
from
Madison, WI
Click here to add this to my saved trials
Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Surgical Treatment of Plantar Fasciitis: Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Status: Enrolling
Updated:  3/28/2016
Step Lively Foot and Ankle Center
mi
from
Dublin, OH
Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Surgical Treatment of Plantar Fasciitis: Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Status: Enrolling
Updated: 3/28/2016
Step Lively Foot and Ankle Center
mi
from
Dublin, OH
Click here to add this to my saved trials
Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Surgical Treatment of Plantar Fasciitis: Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Status: Enrolling
Updated:  3/28/2016
Foot and Ankle Specialists of Central Ohio
mi
from
Gahanna, OH
Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Surgical Treatment of Plantar Fasciitis: Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Status: Enrolling
Updated: 3/28/2016
Foot and Ankle Specialists of Central Ohio
mi
from
Gahanna, OH
Click here to add this to my saved trials
Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Surgical Treatment of Plantar Fasciitis: Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Status: Enrolling
Updated:  3/28/2016
Step Lively Foot and Ankle Center
mi
from
Grove City, OH
Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Surgical Treatment of Plantar Fasciitis: Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Status: Enrolling
Updated: 3/28/2016
Step Lively Foot and Ankle Center
mi
from
Grove City, OH
Click here to add this to my saved trials
Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Surgical Treatment of Plantar Fasciitis: Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Status: Enrolling
Updated:  3/28/2016
Step Lively Foot and Ankle Center
mi
from
Reynoldsburg, OH
Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Surgical Treatment of Plantar Fasciitis: Instep Plantar Fasciotomy With and Without Gastrocnemius Recession
Status: Enrolling
Updated: 3/28/2016
Step Lively Foot and Ankle Center
mi
from
Reynoldsburg, OH
Click here to add this to my saved trials
Comparison of Lokomat and Aquatic Exercise for Individuals With Chronic Incomplete Spinal Cord Injury
Lokomat and Aquatic Therapy in Chronic Motor Incomplete Spinal Cord Injury
Status: Enrolling
Updated:  4/6/2016
Shepherd Center, Virginia C. Crawford Research Institute
mi
from
Atlanta, GA
Comparison of Lokomat and Aquatic Exercise for Individuals With Chronic Incomplete Spinal Cord Injury
Lokomat and Aquatic Therapy in Chronic Motor Incomplete Spinal Cord Injury
Status: Enrolling
Updated: 4/6/2016
Shepherd Center, Virginia C. Crawford Research Institute
mi
from
Atlanta, GA
Click here to add this to my saved trials
Comparison of Lokomat and Aquatic Exercise for Individuals With Chronic Incomplete Spinal Cord Injury
Lokomat and Aquatic Therapy in Chronic Motor Incomplete Spinal Cord Injury
Status: Enrolling
Updated:  4/6/2016
University of Maryland Rehabilitation & Orthopaedic Institute (formerly known as Kernan Hospital)
mi
from
Baltimore, MD
Comparison of Lokomat and Aquatic Exercise for Individuals With Chronic Incomplete Spinal Cord Injury
Lokomat and Aquatic Therapy in Chronic Motor Incomplete Spinal Cord Injury
Status: Enrolling
Updated: 4/6/2016
University of Maryland Rehabilitation & Orthopaedic Institute (formerly known as Kernan Hospital)
mi
from
Baltimore, MD
Click here to add this to my saved trials
[124I]FIAU PET-CT Scanning in Diagnosing Osteomyelitis in Patients With Diabetic Foot Infection
Exploration of the Use of [124I]FIAU Positron Emission Tomography-Computed Tomography Scanning in Diagnosing Osteomyelitis in Patients With Diabetic Foot Infection.
Status: Enrolling
Updated:  4/6/2016
University of Arkansas for Medical Sciences
mi
from
Little Rock, AR
[124I]FIAU PET-CT Scanning in Diagnosing Osteomyelitis in Patients With Diabetic Foot Infection
Exploration of the Use of [124I]FIAU Positron Emission Tomography-Computed Tomography Scanning in Diagnosing Osteomyelitis in Patients With Diabetic Foot Infection.
Status: Enrolling
Updated: 4/6/2016
University of Arkansas for Medical Sciences
mi
from
Little Rock, AR
Click here to add this to my saved trials
[124I]FIAU PET-CT Scanning in Diagnosing Osteomyelitis in Patients With Diabetic Foot Infection
Exploration of the Use of [124I]FIAU Positron Emission Tomography-Computed Tomography Scanning in Diagnosing Osteomyelitis in Patients With Diabetic Foot Infection.
Status: Enrolling
Updated:  4/6/2016
Univ of Pennsylvania
mi
from
Philadelphia, PA
[124I]FIAU PET-CT Scanning in Diagnosing Osteomyelitis in Patients With Diabetic Foot Infection
Exploration of the Use of [124I]FIAU Positron Emission Tomography-Computed Tomography Scanning in Diagnosing Osteomyelitis in Patients With Diabetic Foot Infection.
Status: Enrolling
Updated: 4/6/2016
Univ of Pennsylvania
mi
from
Philadelphia, PA
Click here to add this to my saved trials
[124I]FIAU PET-CT Scanning in Diagnosing Osteomyelitis in Patients With Diabetic Foot Infection
Exploration of the Use of [124I]FIAU Positron Emission Tomography-Computed Tomography Scanning in Diagnosing Osteomyelitis in Patients With Diabetic Foot Infection.
Status: Enrolling
Updated:  4/6/2016
University of Arizona
mi
from
Tucson, AZ
[124I]FIAU PET-CT Scanning in Diagnosing Osteomyelitis in Patients With Diabetic Foot Infection
Exploration of the Use of [124I]FIAU Positron Emission Tomography-Computed Tomography Scanning in Diagnosing Osteomyelitis in Patients With Diabetic Foot Infection.
Status: Enrolling
Updated: 4/6/2016
University of Arizona
mi
from
Tucson, AZ
Click here to add this to my saved trials
Continuous Popliteal Nerve Blocks: Effect of Perineural Catheter Tip Location Relative to the Sciatic Nerve Bifurcation on Postoperative Analgesia
Continuous Popliteal Nerve Blocks: Effect of Perineural Catheter Tip Location Relative to the Sciatic Nerve Bifurcation on Postoperative Analgesia
Status: Enrolling
Updated:  4/7/2016
UCSD Medical Centers (Hillcrest and Thornton)
mi
from
San Diego, CA
Continuous Popliteal Nerve Blocks: Effect of Perineural Catheter Tip Location Relative to the Sciatic Nerve Bifurcation on Postoperative Analgesia
Continuous Popliteal Nerve Blocks: Effect of Perineural Catheter Tip Location Relative to the Sciatic Nerve Bifurcation on Postoperative Analgesia
Status: Enrolling
Updated: 4/7/2016
UCSD Medical Centers (Hillcrest and Thornton)
mi
from
San Diego, CA
Click here to add this to my saved trials
Use Art-assist and Neupogen to Treat Chronic Limb Ischemia
Proteomics and Stem Cell Therapy as a New Vascularization Strategy
Status: Enrolling
Updated:  4/7/2016
University of Chicago
mi
from
Chicago, IL
Use Art-assist and Neupogen to Treat Chronic Limb Ischemia
Proteomics and Stem Cell Therapy as a New Vascularization Strategy
Status: Enrolling
Updated: 4/7/2016
University of Chicago
mi
from
Chicago, IL
Click here to add this to my saved trials
Lumbar Punctures in Neonates: Improving Success Rates and Minimizing Pain
Lumbar Punctures in Neonates: Improving Success Rates and Minimizing Pain
Status: Enrolling
Updated:  4/9/2016
MedStar Georgetown University Hospital
mi
from
Washington,
Lumbar Punctures in Neonates: Improving Success Rates and Minimizing Pain
Lumbar Punctures in Neonates: Improving Success Rates and Minimizing Pain
Status: Enrolling
Updated: 4/9/2016
MedStar Georgetown University Hospital
mi
from
Washington,
Click here to add this to my saved trials
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated:  4/11/2016
Arizona Pain Specialists
mi
from
Scottsdale, AZ
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated: 4/11/2016
Arizona Pain Specialists
mi
from
Scottsdale, AZ
Click here to add this to my saved trials
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated:  4/11/2016
Bluegrass Pain
mi
from
Louisville, KY
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated: 4/11/2016
Bluegrass Pain
mi
from
Louisville, KY
Click here to add this to my saved trials
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated:  4/11/2016
Bright Health Physicians of PIH
mi
from
Whittier, CA
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated: 4/11/2016
Bright Health Physicians of PIH
mi
from
Whittier, CA
Click here to add this to my saved trials
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated:  4/11/2016
Carolina Pain Institute
mi
from
Winston-Salem, NC
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated: 4/11/2016
Carolina Pain Institute
mi
from
Winston-Salem, NC
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SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated:  4/11/2016
Coastal Pain & Spinal Diagnostics Medical Group
mi
from
Carlsbad, CA
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated: 4/11/2016
Coastal Pain & Spinal Diagnostics Medical Group
mi
from
Carlsbad, CA
Click here to add this to my saved trials
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated:  4/11/2016
Comprehensive Pain & Rehabilitation
mi
from
Pascagoula, MS
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated: 4/11/2016
Comprehensive Pain & Rehabilitation
mi
from
Pascagoula, MS
Click here to add this to my saved trials
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated:  4/11/2016
Comprehensive Pain Management Center
mi
from
Campbell, CA
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated: 4/11/2016
Comprehensive Pain Management Center
mi
from
Campbell, CA
Click here to add this to my saved trials
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated:  4/11/2016
Comprehensive Pain Specialists
mi
from
Broomfield, CO
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated: 4/11/2016
Comprehensive Pain Specialists
mi
from
Broomfield, CO
Click here to add this to my saved trials
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated:  4/11/2016
Duke Univ Med Ctr
mi
from
Durham, NC
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated: 4/11/2016
Duke Univ Med Ctr
mi
from
Durham, NC
Click here to add this to my saved trials
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated:  4/11/2016
Granger Pain and Spine
mi
from
West Jordan, UT
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated: 4/11/2016
Granger Pain and Spine
mi
from
West Jordan, UT
Click here to add this to my saved trials
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated:  4/11/2016
H. Lee Moffitt Cancer and Research Institute
mi
from
Tampa, FL
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated: 4/11/2016
H. Lee Moffitt Cancer and Research Institute
mi
from
Tampa, FL
Click here to add this to my saved trials
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated:  4/11/2016
Holy Cross Orthopedics
mi
from
Fort Lauderdale, FL
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation)Study for the Treatment of Chronic Low Back and Leg Pain
Status: Enrolling
Updated: 4/11/2016
Holy Cross Orthopedics
mi
from
Fort Lauderdale, FL
Click here to add this to my saved trials