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 Tolerant Kidney Transplant Recipients
Identification and Mechanistic Investigations of Tolerant Transplant Recipients
Status: Enrolling
Updated:  3/3/2016
University of Wisconsin
mi
from
Madison, WI
Study of Tolerant Kidney Transplant Recipients
Identification and Mechanistic Investigations of Tolerant Transplant Recipients
Status: Enrolling
Updated: 3/3/2016
University of Wisconsin
mi
from
Madison, WI
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Study of Tolerant Kidney Transplant Recipients
Identification and Mechanistic Investigations of Tolerant Transplant Recipients
Status: Enrolling
Updated:  3/3/2016
NIH Clinical Center
mi
from
Bethesda, MD
Study of Tolerant Kidney Transplant Recipients
Identification and Mechanistic Investigations of Tolerant Transplant Recipients
Status: Enrolling
Updated: 3/3/2016
NIH Clinical Center
mi
from
Bethesda, MD
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Study of Tolerant Kidney Transplant Recipients
Identification and Mechanistic Investigations of Tolerant Transplant Recipients
Status: Enrolling
Updated:  3/3/2016
Swedish Medical Center
mi
from
Seattle, WA
Study of Tolerant Kidney Transplant Recipients
Identification and Mechanistic Investigations of Tolerant Transplant Recipients
Status: Enrolling
Updated: 3/3/2016
Swedish Medical Center
mi
from
Seattle, WA
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Effects of Ankle Support on Muscle Activation and Function
Effects of Ankle Support on Muscle Activation and Function
Status: Enrolling
Updated:  3/3/2016
Creighton University
mi
from
Omaha, NE
Effects of Ankle Support on Muscle Activation and Function
Effects of Ankle Support on Muscle Activation and Function
Status: Enrolling
Updated: 3/3/2016
Creighton University
mi
from
Omaha, NE
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Observational Study to Evaluate Mechanisms of Aromatase Inhibitor Associated Musculoskeletal Symptoms
Prospective Observational Study of Breast Cancer Patients Starting Therapy With an AI to Evaluate Mechanisms Underlying Development of Aromatase Inhibitor Associated Musculoskeletal Symptoms
Status: Enrolling
Updated:  3/3/2016
University of Michigan Comprehensive Cancer Center
mi
from
Ann Arbor, MI
Observational Study to Evaluate Mechanisms of Aromatase Inhibitor Associated Musculoskeletal Symptoms
Prospective Observational Study of Breast Cancer Patients Starting Therapy With an AI to Evaluate Mechanisms Underlying Development of Aromatase Inhibitor Associated Musculoskeletal Symptoms
Status: Enrolling
Updated: 3/3/2016
University of Michigan Comprehensive Cancer Center
mi
from
Ann Arbor, MI
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Addition of Etanercept and Extracorporeal Photopheresis (ECP) to Standard Graft-Versus-Host Disease (GVHD) Prophylaxis in Stem Cell Transplant
Addition of Etanercept and Extracorporeal Photopheresis to Standard GVHD Prophylaxis in Patients Undergoing Reduced Intensity Unrelated Donor Hematopoietic Stem Cell Transplant
Status: Enrolling
Updated:  3/8/2016
University of Michigan Cancer Center
mi
from
Ann Arbor, MI
Addition of Etanercept and Extracorporeal Photopheresis (ECP) to Standard Graft-Versus-Host Disease (GVHD) Prophylaxis in Stem Cell Transplant
Addition of Etanercept and Extracorporeal Photopheresis to Standard GVHD Prophylaxis in Patients Undergoing Reduced Intensity Unrelated Donor Hematopoietic Stem Cell Transplant
Status: Enrolling
Updated: 3/8/2016
University of Michigan Cancer Center
mi
from
Ann Arbor, MI
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Efficacy of Levetiracetam in Oromandibular and Cranial Dystonia
Efficacy of Levetiracetam in Oromandibular and Cranial Dystonia: A Randomized, Double-Blind Placebo-Controlled Cross-Over Study
Status: Enrolling
Updated:  3/9/2016
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
Efficacy of Levetiracetam in Oromandibular and Cranial Dystonia
Efficacy of Levetiracetam in Oromandibular and Cranial Dystonia: A Randomized, Double-Blind Placebo-Controlled Cross-Over Study
Status: Enrolling
Updated: 3/9/2016
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
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Continuous Femoral Nerve Block With a Tibial Plateau Fracture
Postoperative Pain Management With a Continuous Femoral Nerve Block in Patients With a Tibial Plateau Fracture
Status: Enrolling
Updated:  3/11/2016
University of Utah
mi
from
Salt Lake City, UT
Continuous Femoral Nerve Block With a Tibial Plateau Fracture
Postoperative Pain Management With a Continuous Femoral Nerve Block in Patients With a Tibial Plateau Fracture
Status: Enrolling
Updated: 3/11/2016
University of Utah
mi
from
Salt Lake City, UT
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Patient Registry to Observe Outcomes Following Implantation of the VariLift Interbody Fusion Device
VariLift Lumbar and Cervical Patient Registry
Status: Enrolling
Updated:  3/14/2016
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Patient Registry to Observe Outcomes Following Implantation of the VariLift Interbody Fusion Device
VariLift Lumbar and Cervical Patient Registry
Status: Enrolling
Updated: 3/14/2016
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
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Patient Registry to Observe Outcomes Following Implantation of the VariLift Interbody Fusion Device
VariLift Lumbar and Cervical Patient Registry
Status: Enrolling
Updated:  3/14/2016
Foundation Surgical Hospital
mi
from
San Antonio, TX
Patient Registry to Observe Outcomes Following Implantation of the VariLift Interbody Fusion Device
VariLift Lumbar and Cervical Patient Registry
Status: Enrolling
Updated: 3/14/2016
Foundation Surgical Hospital
mi
from
San Antonio, TX
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Patient Registry to Observe Outcomes Following Implantation of the VariLift Interbody Fusion Device
VariLift Lumbar and Cervical Patient Registry
Status: Enrolling
Updated:  3/14/2016
Methodist Hospital
mi
from
San Antonio, TX
Patient Registry to Observe Outcomes Following Implantation of the VariLift Interbody Fusion Device
VariLift Lumbar and Cervical Patient Registry
Status: Enrolling
Updated: 3/14/2016
Methodist Hospital
mi
from
San Antonio, TX
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Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated:  3/14/2016
Palo Alto Medical Foundation
mi
from
Palo Alto, CA
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated: 3/14/2016
Palo Alto Medical Foundation
mi
from
Palo Alto, CA
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Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated:  3/14/2016
Alvarado Orthopedic Clinic
mi
from
San Diego, CA
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated: 3/14/2016
Alvarado Orthopedic Clinic
mi
from
San Diego, CA
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Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated:  3/14/2016
American Health Network
mi
from
Avon, IN
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated: 3/14/2016
American Health Network
mi
from
Avon, IN
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Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated:  3/14/2016
Raliegh Orthopedic Research Foundation
mi
from
Raleigh, NC
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
Status: Enrolling
Updated: 3/14/2016
Raliegh Orthopedic Research Foundation
mi
from
Raleigh, NC
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Spine Patient Outcomes Registry for Biomet/EBI
BIOMET/EBI Spine Patient Outcomes Registry
Status: Enrolling
Updated:  3/14/2016
Neurological Surgery Associates
mi
from
Little Rock, AR
Spine Patient Outcomes Registry for Biomet/EBI
BIOMET/EBI Spine Patient Outcomes Registry
Status: Enrolling
Updated: 3/14/2016
Neurological Surgery Associates
mi
from
Little Rock, AR
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Spine Patient Outcomes Registry for Biomet/EBI
BIOMET/EBI Spine Patient Outcomes Registry
Status: Enrolling
Updated:  3/14/2016
Florida Orthopedics Association
mi
from
Orange City, FL
Spine Patient Outcomes Registry for Biomet/EBI
BIOMET/EBI Spine Patient Outcomes Registry
Status: Enrolling
Updated: 3/14/2016
Florida Orthopedics Association
mi
from
Orange City, FL
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Spine Patient Outcomes Registry for Biomet/EBI
BIOMET/EBI Spine Patient Outcomes Registry
Status: Enrolling
Updated:  3/14/2016
CNS Healthcare
mi
from
Akron, OH
Spine Patient Outcomes Registry for Biomet/EBI
BIOMET/EBI Spine Patient Outcomes Registry
Status: Enrolling
Updated: 3/14/2016
CNS Healthcare
mi
from
Akron, OH
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Spine Patient Outcomes Registry for Biomet/EBI
BIOMET/EBI Spine Patient Outcomes Registry
Status: Enrolling
Updated:  3/14/2016
Oklahoma Spine and Brain
mi
from
Tulsa, OK
Spine Patient Outcomes Registry for Biomet/EBI
BIOMET/EBI Spine Patient Outcomes Registry
Status: Enrolling
Updated: 3/14/2016
Oklahoma Spine and Brain
mi
from
Tulsa, OK
Click here to add this to my saved trials
Spine Patient Outcomes Registry for Biomet/EBI
BIOMET/EBI Spine Patient Outcomes Registry
Status: Enrolling
Updated:  3/14/2016
Pottstown Memorial Medical Center
mi
from
Pottstown, PA
Spine Patient Outcomes Registry for Biomet/EBI
BIOMET/EBI Spine Patient Outcomes Registry
Status: Enrolling
Updated: 3/14/2016
Pottstown Memorial Medical Center
mi
from
Pottstown, PA
Click here to add this to my saved trials
Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal Instability
A Multicenter Prospective Patient Outcome Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal Instability
Status: Enrolling
Updated:  3/14/2016
Alvarado Orthopedic Clinic
mi
from
San Diego, CA
Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal Instability
A Multicenter Prospective Patient Outcome Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal Instability
Status: Enrolling
Updated: 3/14/2016
Alvarado Orthopedic Clinic
mi
from
San Diego, CA
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Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal Instability
A Multicenter Prospective Patient Outcome Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal Instability
Status: Enrolling
Updated:  3/14/2016
Rogozinski Orthopedic Clinic
mi
from
Jacksonville, FL
Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal Instability
A Multicenter Prospective Patient Outcome Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal Instability
Status: Enrolling
Updated: 3/14/2016
Rogozinski Orthopedic Clinic
mi
from
Jacksonville, FL
Click here to add this to my saved trials
Patient Satisfaction With Pain Relief After Ambulatory Hand Surgery
Satisfaction With Pain Relief After Carpal Tunnel Release Surgery
Status: Enrolling
Updated:  3/15/2016
Massachusetts General Hospital
mi
from
Boston, MA
Patient Satisfaction With Pain Relief After Ambulatory Hand Surgery
Satisfaction With Pain Relief After Carpal Tunnel Release Surgery
Status: Enrolling
Updated: 3/15/2016
Massachusetts General Hospital
mi
from
Boston, MA
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A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated:  3/15/2016
St. Joseph's Hospital and Medical Center
mi
from
Phoenix, AZ
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated: 3/15/2016
St. Joseph's Hospital and Medical Center
mi
from
Phoenix, AZ
Click here to add this to my saved trials
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated:  3/15/2016
University of Cincinnati Mayfield Clinic and Spine Institute
mi
from
Cincinnati, OH
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated: 3/15/2016
University of Cincinnati Mayfield Clinic and Spine Institute
mi
from
Cincinnati, OH
Click here to add this to my saved trials
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated:  3/15/2016
Thomas Jefferson University Hospital
mi
from
Philadelphia, PA
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated: 3/15/2016
Thomas Jefferson University Hospital
mi
from
Philadelphia, PA
Click here to add this to my saved trials
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated:  3/15/2016
Univ.of Virginia Health System
mi
from
Charlottesville, VA
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated: 3/15/2016
Univ.of Virginia Health System
mi
from
Charlottesville, VA
Click here to add this to my saved trials
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated:  3/15/2016
University of Washington; Harborview Medical Center
mi
from
Seattle, WA
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated: 3/15/2016
University of Washington; Harborview Medical Center
mi
from
Seattle, WA
Click here to add this to my saved trials
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated:  3/15/2016
Sunnybrooke Health Sciences Centre
mi
from
Toronto,
A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries
A Phase I/IIa Dose-Ranging Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of BA-210 and the Neurological Status of Patients Following Administration of a Single Extradural Application of Cethrin During Surgery for Acute Thoracic and Cervical Spinal Cord Injury
Status: Enrolling
Updated: 3/15/2016
Sunnybrooke Health Sciences Centre
mi
from
Toronto,
Click here to add this to my saved trials
Effects of Frailty, Sarcopenia and Muscle Wasting on Outcomes of Patients in the Surgical Intensive Care Unit
Ultrasound Assessment of Muscle to Quantify Frailty.
Status: Enrolling
Updated:  3/16/2016
Massachusetts General Hospital
mi
from
Boston, MA
Effects of Frailty, Sarcopenia and Muscle Wasting on Outcomes of Patients in the Surgical Intensive Care Unit
Ultrasound Assessment of Muscle to Quantify Frailty.
Status: Enrolling
Updated: 3/16/2016
Massachusetts General Hospital
mi
from
Boston, MA
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Dexmedetomidine vs Propofol TIVA (Total Intravenous Anesthesia) and Interscalene Block
Dexmedetomidine vs Propofol TIVA and Interscalene Block for Shoulder Surgeries in a Beach Chair Sitting Position
Status: Enrolling
Updated:  3/17/2016
Maimonides Medical Center
mi
from
Brooklyn, NY
Dexmedetomidine vs Propofol TIVA (Total Intravenous Anesthesia) and Interscalene Block
Dexmedetomidine vs Propofol TIVA and Interscalene Block for Shoulder Surgeries in a Beach Chair Sitting Position
Status: Enrolling
Updated: 3/17/2016
Maimonides Medical Center
mi
from
Brooklyn, NY
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Effectiveness of Controlled-Release Morphine for Chronic Neuropathic Pain After Spinal Cord Injury
Effectiveness of Controlled-Release Morphine for Chronic Neuropathic Pain After Spinal Cord Injury
Status: Enrolling
Updated:  3/18/2016
Mount Sinai School of Medicine
mi
from
New York, NY
Effectiveness of Controlled-Release Morphine for Chronic Neuropathic Pain After Spinal Cord Injury
Effectiveness of Controlled-Release Morphine for Chronic Neuropathic Pain After Spinal Cord Injury
Status: Enrolling
Updated: 3/18/2016
Mount Sinai School of Medicine
mi
from
New York, NY
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Liposomal Bupivacaine in Total Knee Arthroplasty
Analgesic Efficacy of Liposomal Bupivacaine in Total Knee Arthroplasty
Status: Enrolling
Updated:  3/18/2016
Miller Orthopedic Specialists
mi
from
Council Bluffs, IA
Liposomal Bupivacaine in Total Knee Arthroplasty
Analgesic Efficacy of Liposomal Bupivacaine in Total Knee Arthroplasty
Status: Enrolling
Updated: 3/18/2016
Miller Orthopedic Specialists
mi
from
Council Bluffs, IA
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Novel Stimulation Patterns for the Treatment of Dystonia
Novel Stimulation Patterns and Personalized Deep Brain Stimulation for the Treatment of Dystonia
Status: Enrolling
Updated:  3/18/2016
Center for Movement Disorders and Neurorestoration
mi
from
Gainesville, FL
Novel Stimulation Patterns for the Treatment of Dystonia
Novel Stimulation Patterns and Personalized Deep Brain Stimulation for the Treatment of Dystonia
Status: Enrolling
Updated: 3/18/2016
Center for Movement Disorders and Neurorestoration
mi
from
Gainesville, FL
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Efficacy and Safety of Zoledronic Acid in Acute Spinal Cord Injury: Prevention of Bone Loss
Efficacy and Safety of Zoledronic Acid in Acute Spinal Cord Injury: Prevention of Bone Loss
Status: Enrolling
Updated:  3/21/2016
Rehabilitation Institute of Chicago
mi
from
Chicago, IL
Efficacy and Safety of Zoledronic Acid in Acute Spinal Cord Injury: Prevention of Bone Loss
Efficacy and Safety of Zoledronic Acid in Acute Spinal Cord Injury: Prevention of Bone Loss
Status: Enrolling
Updated: 3/21/2016
Rehabilitation Institute of Chicago
mi
from
Chicago, IL
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Study of A Long Lasting Local Anesthestic for Hand, Wrist or Finger Surgery
Exparel (Bupivacaine Liposome Injectable Suspension) for Distal Upper Extremity Blocks in Orthopedic Surgery
Status: Enrolling
Updated:  3/21/2016
Ochsner Clinic Foundation
mi
from
New Orleans, LA
Study of A Long Lasting Local Anesthestic for Hand, Wrist or Finger Surgery
Exparel (Bupivacaine Liposome Injectable Suspension) for Distal Upper Extremity Blocks in Orthopedic Surgery
Status: Enrolling
Updated: 3/21/2016
Ochsner Clinic Foundation
mi
from
New Orleans, LA
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Comparing Two Injection Sites of Local Anesthetic for Hand Surgery
A Comparison Of Distal Peripheral Nerve Blockade Versus Traditional Proximal Approaches For Hand Surgery
Status: Enrolling
Updated:  3/21/2016
Ochsner Clinic Foundation
mi
from
New Orleans, LA
Comparing Two Injection Sites of Local Anesthetic for Hand Surgery
A Comparison Of Distal Peripheral Nerve Blockade Versus Traditional Proximal Approaches For Hand Surgery
Status: Enrolling
Updated: 3/21/2016
Ochsner Clinic Foundation
mi
from
New Orleans, LA
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Electrical Impedance Myography and Ultrasound as Biomarkers of Duchenne Muscular Dystrophy
Electrical Impedance Myography and Ultrasound as Biomarkers of Duchenne Muscular Dystrophy
Status: Enrolling
Updated:  3/23/2016
Children's Hospital Boston
mi
from
Boston, MA
Electrical Impedance Myography and Ultrasound as Biomarkers of Duchenne Muscular Dystrophy
Electrical Impedance Myography and Ultrasound as Biomarkers of Duchenne Muscular Dystrophy
Status: Enrolling
Updated: 3/23/2016
Children's Hospital Boston
mi
from
Boston, MA
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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
Valley Pain Consultants
mi
from
Phoenix, AZ
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
Valley Pain Consultants
mi
from
Phoenix, AZ
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
Pain Medicine Associates
mi
from
Huntington Beach, CA
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
Pain Medicine Associates
mi
from
Huntington Beach, CA
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
Compass Research LLC
mi
from
Orlando, FL
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
Compass Research LLC
mi
from
Orlando, FL
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
Columbia Interventional Pain Center, LLP
mi
from
Columbia, 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
Columbia Interventional Pain Center, LLP
mi
from
Columbia, 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
Ohio State University
mi
from
Columbus, 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
Ohio State University
mi
from
Columbus, OH
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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
Summa Western Reserve Hospital
mi
from
Cuyahoga Falls, 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
Summa Western Reserve Hospital
mi
from
Cuyahoga Falls, 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
DNA Advanced Pain Treatment Center
mi
from
Greensburg, 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
DNA Advanced Pain Treatment Center
mi
from
Greensburg, 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
HOPE Research Institute
mi
from
Phoenix, AZ
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
HOPE Research Institute
mi
from
Phoenix, AZ
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
Coastal Pain Research
mi
from
Carlsbad, CA
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
Coastal Pain Research
mi
from
Carlsbad, CA
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
Florida Pain Institute
mi
from
Merritt Island, FL
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
Florida Pain Institute
mi
from
Merritt Island, FL
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
Advanced Medicine and Pain Management Research
mi
from
Miami, FL
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
Advanced Medicine and Pain Management Research
mi
from
Miami, FL
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
Emory University School of Medicine
mi
from
Atlanta, GA
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
Emory University School of Medicine
mi
from
Atlanta, GA
Click here to add this to my saved trials