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
33,560
archived clinical trials in
Neurology

NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Multiple Sclerosis Experiencing Fatigue or Sleepiness
NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Relapsing Forms of Multiple Sclerosis Experiencing Fatigue or Sleepiness
Status: Enrolling
Updated:  5/2/2012
Cornerstone Neurology
mi
from
High Point, NC
NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Multiple Sclerosis Experiencing Fatigue or Sleepiness
NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Relapsing Forms of Multiple Sclerosis Experiencing Fatigue or Sleepiness
Status: Enrolling
Updated: 5/2/2012
Cornerstone Neurology
mi
from
High Point, NC
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NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Multiple Sclerosis Experiencing Fatigue or Sleepiness
NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Relapsing Forms of Multiple Sclerosis Experiencing Fatigue or Sleepiness
Status: Enrolling
Updated:  5/2/2012
Providence Brain Institute
mi
from
Portland, OR
NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Multiple Sclerosis Experiencing Fatigue or Sleepiness
NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Relapsing Forms of Multiple Sclerosis Experiencing Fatigue or Sleepiness
Status: Enrolling
Updated: 5/2/2012
Providence Brain Institute
mi
from
Portland, OR
Click here to add this to my saved trials
NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Multiple Sclerosis Experiencing Fatigue or Sleepiness
NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Relapsing Forms of Multiple Sclerosis Experiencing Fatigue or Sleepiness
Status: Enrolling
Updated:  5/2/2012
Hope Neurology
mi
from
Knoxville, TN
NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Multiple Sclerosis Experiencing Fatigue or Sleepiness
NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Relapsing Forms of Multiple Sclerosis Experiencing Fatigue or Sleepiness
Status: Enrolling
Updated: 5/2/2012
Hope Neurology
mi
from
Knoxville, TN
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Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated:  5/3/2012
University of Southern California Keck School of Medicine Memory and Aging Center
mi
from
Los Angeles, CA
Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated: 5/3/2012
University of Southern California Keck School of Medicine Memory and Aging Center
mi
from
Los Angeles, CA
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Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated:  5/3/2012
VA Palo Alto Health Care System
mi
from
Palo Alto, CA
Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated: 5/3/2012
VA Palo Alto Health Care System
mi
from
Palo Alto, CA
Click here to add this to my saved trials
Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated:  5/3/2012
Johns Hopkins University
mi
from
Baltimore, MD
Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated: 5/3/2012
Johns Hopkins University
mi
from
Baltimore, MD
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Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated:  5/3/2012
Columbia University
mi
from
New York, NY
Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated: 5/3/2012
Columbia University
mi
from
New York, NY
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Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated:  5/3/2012
Monroe Community Hospital
mi
from
Rochester, NY
Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated: 5/3/2012
Monroe Community Hospital
mi
from
Rochester, NY
Click here to add this to my saved trials
Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated:  5/3/2012
University of Pennsylvania, Section of Geriatric Psychiatry, Ralston House
mi
from
Philadelphia, PA
Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated: 5/3/2012
University of Pennsylvania, Section of Geriatric Psychiatry, Ralston House
mi
from
Philadelphia, PA
Click here to add this to my saved trials
Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated:  5/3/2012
Medical University of South Carolina Alzheimer's Research and Clinical Programs
mi
from
Charleston, SC
Citalopram for Agitation in Alzheimer's Disease
A Multi-Center Randomized Placebo-Controlled Clinical Trial Study of Citalopram for the Treatment of Agitation in Alzheimer's Disease
Status: Enrolling
Updated: 5/3/2012
Medical University of South Carolina Alzheimer's Research and Clinical Programs
mi
from
Charleston, SC
Click here to add this to my saved trials
Hyperlipidemia and Statin Therapy in Amyotrophic Lateral Sclerosis
Cohort Study of the Relationship of Hyperlipidemia and Statin Therapy on Survival and Disease Progresssion in Amyotrophic Lateral Sclerosis
Status: Enrolling
Updated:  5/3/2012
Methodist Neurological Institute
mi
from
Houston, TX
Hyperlipidemia and Statin Therapy in Amyotrophic Lateral Sclerosis
Cohort Study of the Relationship of Hyperlipidemia and Statin Therapy on Survival and Disease Progresssion in Amyotrophic Lateral Sclerosis
Status: Enrolling
Updated: 5/3/2012
Methodist Neurological Institute
mi
from
Houston, TX
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Venous Obstruction in Neurodegenerative Disorders Research Registry
Venous Obstruction in Neurodegenerative Disorders Research Registry
Status: Enrolling
Updated:  5/5/2012
Synergy Health Concepts, Inc.
mi
from
Newport Beach, CA
Venous Obstruction in Neurodegenerative Disorders Research Registry
Venous Obstruction in Neurodegenerative Disorders Research Registry
Status: Enrolling
Updated: 5/5/2012
Synergy Health Concepts, Inc.
mi
from
Newport Beach, CA
Click here to add this to my saved trials
Mind-Body Skills Groups for the Treatment of War Zone Stress in Military and Veteran Populations
A Randomized Controlled Study of Mind-Body Skills Groups for Treatment of War Zone Stress in Military and Veteran Populations
Status: Enrolling
Updated:  5/7/2012
Southeast Louisiana Veterans Healthcare System
mi
from
New Orleans, LA
Mind-Body Skills Groups for the Treatment of War Zone Stress in Military and Veteran Populations
A Randomized Controlled Study of Mind-Body Skills Groups for Treatment of War Zone Stress in Military and Veteran Populations
Status: Enrolling
Updated: 5/7/2012
Southeast Louisiana Veterans Healthcare System
mi
from
New Orleans, LA
Click here to add this to my saved trials
Nebivolol in the Supine Hypertension of Autonomic Failure
Effect of Nebivolol on Blood Pressure in a Model of Hypertension Sensitive to Potentiation of Nitric Oxide Bioactivity
Status: Enrolling
Updated:  5/10/2012
Vanderbilt University
mi
from
Nashville, TN
Nebivolol in the Supine Hypertension of Autonomic Failure
Effect of Nebivolol on Blood Pressure in a Model of Hypertension Sensitive to Potentiation of Nitric Oxide Bioactivity
Status: Enrolling
Updated: 5/10/2012
Vanderbilt University
mi
from
Nashville, TN
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Efficacy of Tyrosine in Restless Legs Syndrome
Pilot Study of the Efficacy of Tyrosine in Restless Legs Syndrome
Status: Enrolling
Updated:  5/10/2012
Seton Family of Hospitals
mi
from
Austin, TX
Efficacy of Tyrosine in Restless Legs Syndrome
Pilot Study of the Efficacy of Tyrosine in Restless Legs Syndrome
Status: Enrolling
Updated: 5/10/2012
Seton Family of Hospitals
mi
from
Austin, TX
Click here to add this to my saved trials
A Study Comparing Long-acting Methylphenidate (ConcertaTM) vs. Placebo in the Treatment of Memory Loss Due to HIV
Phase III, Placebo-Controlled, Double-Blind Crossover Study of Slow-Release Methylphenidate (Concerta ™) for Treatment of HIV Associated Neurocognitive Disorder
Status: Enrolling
Updated:  5/14/2012
UCLA CARE Clinic
mi
from
Los Angeles, CA
A Study Comparing Long-acting Methylphenidate (ConcertaTM) vs. Placebo in the Treatment of Memory Loss Due to HIV
Phase III, Placebo-Controlled, Double-Blind Crossover Study of Slow-Release Methylphenidate (Concerta ™) for Treatment of HIV Associated Neurocognitive Disorder
Status: Enrolling
Updated: 5/14/2012
UCLA CARE Clinic
mi
from
Los Angeles, CA
Click here to add this to my saved trials
Effect of Exercise in OI
Effects of Exercise in Orthostatic Intolerance
Status: Enrolling
Updated:  5/18/2012
Vanderbilt University Medical Center
mi
from
Nashville, TN
Effect of Exercise in OI
Effects of Exercise in Orthostatic Intolerance
Status: Enrolling
Updated: 5/18/2012
Vanderbilt University Medical Center
mi
from
Nashville, TN
Click here to add this to my saved trials
Modulation of Cerebral Blood Flow Using Quercetin, a Nutritional Supplement
Hypoxia-inducible Transcription Factor 1 (HIF-1) in Vascular Aging
Status: Enrolling
Updated:  5/22/2012
Brigham and Women's Hosp
mi
from
Boston, MA
Modulation of Cerebral Blood Flow Using Quercetin, a Nutritional Supplement
Hypoxia-inducible Transcription Factor 1 (HIF-1) in Vascular Aging
Status: Enrolling
Updated: 5/22/2012
Brigham and Women's Hosp
mi
from
Boston, MA
Click here to add this to my saved trials
Noninvasive Monitoring of Cerebral Blood Flow Autoregulation in Patients With Traumatic Brain Injury (TBI)
Pilot (Feasibility) Study of New Portable Monitor for Continuous Assessment of Cerebral Blood Flow (CBF) Autoregulation in Patients With Moderate to Severe Traumatic Brain Injury (TBI)
Status: Enrolling
Updated:  5/23/2012
LA County/USC Medical Center
mi
from
Los Angeles, CA
Noninvasive Monitoring of Cerebral Blood Flow Autoregulation in Patients With Traumatic Brain Injury (TBI)
Pilot (Feasibility) Study of New Portable Monitor for Continuous Assessment of Cerebral Blood Flow (CBF) Autoregulation in Patients With Moderate to Severe Traumatic Brain Injury (TBI)
Status: Enrolling
Updated: 5/23/2012
LA County/USC Medical Center
mi
from
Los Angeles, CA
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Early Mobilization of Ischemic Stroke Patients Within 24-hours After Intravenous-Tissue Plasminogen Activator (IV-tPA)
Early Mobilization of Ischemic Stroke Patients Within 24-hours After Intravenous-tPA Infusion.
Status: Enrolling
Updated:  5/24/2012
Mayo Clinic Hospital
mi
from
Jacksonville, FL
Early Mobilization of Ischemic Stroke Patients Within 24-hours After Intravenous-Tissue Plasminogen Activator (IV-tPA)
Early Mobilization of Ischemic Stroke Patients Within 24-hours After Intravenous-tPA Infusion.
Status: Enrolling
Updated: 5/24/2012
Mayo Clinic Hospital
mi
from
Jacksonville, FL
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RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
Status: Enrolling
Updated:  5/25/2012
Clinical Research Facility
mi
from
Washington,
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
Status: Enrolling
Updated: 5/25/2012
Clinical Research Facility
mi
from
Washington,
Click here to add this to my saved trials
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
Status: Enrolling
Updated:  5/25/2012
Clinical Research Facility
mi
from
Park Ridge, IL
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
Status: Enrolling
Updated: 5/25/2012
Clinical Research Facility
mi
from
Park Ridge, IL
Click here to add this to my saved trials
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
Status: Enrolling
Updated:  5/25/2012
Clinical Research Facility
mi
from
Chattanooga, TN
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
Status: Enrolling
Updated: 5/25/2012
Clinical Research Facility
mi
from
Chattanooga, TN
Click here to add this to my saved trials
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
Status: Enrolling
Updated:  5/25/2012
Clinical Research Facility
mi
from
Dallas, TX
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR)
Status: Enrolling
Updated: 5/25/2012
Clinical Research Facility
mi
from
Dallas, TX
Click here to add this to my saved trials
Safety Study of HPP593 in Subjects During and After Limb Immobilization
A Randomized, Double-blind, Placebo Controlled, Phase I Study to Evaluate the Safety and Tolerability of 28 Day Treatment With HPP593 Capsules in Healthy Volunteers During and After Limb Immobilization
Status: Enrolling
Updated:  5/25/2012
Washington University School of Medicine Division of Geriatrics and Nutritional Studies
mi
from
St. Louis, MO
Safety Study of HPP593 in Subjects During and After Limb Immobilization
A Randomized, Double-blind, Placebo Controlled, Phase I Study to Evaluate the Safety and Tolerability of 28 Day Treatment With HPP593 Capsules in Healthy Volunteers During and After Limb Immobilization
Status: Enrolling
Updated: 5/25/2012
Washington University School of Medicine Division of Geriatrics and Nutritional Studies
mi
from
St. Louis, MO
Click here to add this to my saved trials
The Effect of Clevidipine on Intracranial Pressure and Cerebral Perfusion Pressure (CCP) in Brain Injured Patients
Effect of Clevidipine on Intracranial Pressure, Cerebral Blood Flow, Brain Tissue Oxygenation and Brain Cellular Metabolism in Severely Hypertensive Patients With Acute Brain Injury
Status: Enrolling
Updated:  5/25/2012
Columbia University Medical Center
mi
from
New York, NY
The Effect of Clevidipine on Intracranial Pressure and Cerebral Perfusion Pressure (CCP) in Brain Injured Patients
Effect of Clevidipine on Intracranial Pressure, Cerebral Blood Flow, Brain Tissue Oxygenation and Brain Cellular Metabolism in Severely Hypertensive Patients With Acute Brain Injury
Status: Enrolling
Updated: 5/25/2012
Columbia University Medical Center
mi
from
New York, NY
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Vasospasm in Pediatric Traumatic Brain Injury
Measuring Vasospasm, Biomarkers, and Neurocognitive Outcomes in Pediatric Traumatic Brain Injury
Status: Enrolling
Updated:  5/29/2012
Duke Univ Med Ctr
mi
from
Durham, NC
Vasospasm in Pediatric Traumatic Brain Injury
Measuring Vasospasm, Biomarkers, and Neurocognitive Outcomes in Pediatric Traumatic Brain Injury
Status: Enrolling
Updated: 5/29/2012
Duke Univ Med Ctr
mi
from
Durham, NC
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Chronic Fatigue Syndrome: A Presumptive Mitochondrial Disorder
Chronic Fatigue Syndrome: Correction of Mitochondrial Dysfunction by Conditioning Exercise and Nutraceutical Therapy.
Status: Enrolling
Updated:  5/31/2012
Columbia University Department of Clinical Genetics
mi
from
New York, NY
Chronic Fatigue Syndrome: A Presumptive Mitochondrial Disorder
Chronic Fatigue Syndrome: Correction of Mitochondrial Dysfunction by Conditioning Exercise and Nutraceutical Therapy.
Status: Enrolling
Updated: 5/31/2012
Columbia University Department of Clinical Genetics
mi
from
New York, NY
Click here to add this to my saved trials
Comparative Anti-Reflux Procedures in Neurologically Impaired Children
Comparative Anti-Reflux Procedures in Neurologically Impaired Children
Status: Enrolling
Updated:  6/1/2012
Primary Children's Medical Center
mi
from
Salt Lake City, UT
Comparative Anti-Reflux Procedures in Neurologically Impaired Children
Comparative Anti-Reflux Procedures in Neurologically Impaired Children
Status: Enrolling
Updated: 6/1/2012
Primary Children's Medical Center
mi
from
Salt Lake City, UT
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Study of Rifaximin in Minimal Hepatic Encephalopathy
Effect of Rifaximin Therapy on Brain Activation in Patients With Minimal Hepatic Encephalopathy Using Functional MR, MR Spectroscopy and Diffusion Tensor Imaging: a Prospective Trial
Status: Enrolling
Updated:  6/1/2012
Hunter Holmes McGuire VA Medical Center
mi
from
Richmond, VA
Study of Rifaximin in Minimal Hepatic Encephalopathy
Effect of Rifaximin Therapy on Brain Activation in Patients With Minimal Hepatic Encephalopathy Using Functional MR, MR Spectroscopy and Diffusion Tensor Imaging: a Prospective Trial
Status: Enrolling
Updated: 6/1/2012
Hunter Holmes McGuire VA Medical Center
mi
from
Richmond, VA
Click here to add this to my saved trials
MRI Study of Tic Remission in Tourette Syndrome
Neuroimaging to Elucidate the Mechanism of Tic Resolution in Tourette Syndrome
Status: Enrolling
Updated:  6/1/2012
University of Utah
mi
from
Salt Lake City, UT
MRI Study of Tic Remission in Tourette Syndrome
Neuroimaging to Elucidate the Mechanism of Tic Resolution in Tourette Syndrome
Status: Enrolling
Updated: 6/1/2012
University of Utah
mi
from
Salt Lake City, UT
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A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated:  6/1/2012
University of California at San Diego
mi
from
San Diego, CA
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated: 6/1/2012
University of California at San Diego
mi
from
San Diego, CA
Click here to add this to my saved trials
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated:  6/1/2012
University of California, Davis Medical Center
mi
from
Sacramento, CA
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated: 6/1/2012
University of California, Davis Medical Center
mi
from
Sacramento, CA
Click here to add this to my saved trials
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated:  6/1/2012
Washington University
mi
from
St. Louis, MO
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated: 6/1/2012
Washington University
mi
from
St. Louis, MO
Click here to add this to my saved trials
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated:  6/1/2012
University of Rochester
mi
from
Rochester, NY
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated: 6/1/2012
University of Rochester
mi
from
Rochester, NY
Click here to add this to my saved trials
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated:  6/1/2012
Wake Forest School of Medicine
mi
from
Winston-Salem, NC
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated: 6/1/2012
Wake Forest School of Medicine
mi
from
Winston-Salem, NC
Click here to add this to my saved trials
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated:  6/1/2012
University of Texas Southwestern Medical Center
mi
from
Dallas, TX
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated: 6/1/2012
University of Texas Southwestern Medical Center
mi
from
Dallas, TX
Click here to add this to my saved trials
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated:  6/1/2012
Baylor College of Medicine
mi
from
Houston, TX
A Open-label Food Effect Study With SEN0014196 in Subjects With Huntington Disease
A Phase 1b, Open-label, Parallel-group Study in Subjects With Huntington Disease to Assess the Safety, Tolerability, and Fed/Fasted Pharmacokinetics of Repeated Oral Doses of SEN0014196
Status: Enrolling
Updated: 6/1/2012
Baylor College of Medicine
mi
from
Houston, TX
Click here to add this to my saved trials
How Well do Patients With Traumatic Brain Injury Learn New Material Using Learning Styles in Online Science Classrooms?
Instructional Design Strategies to Support Adult Patients/Students (Civilian & Military) With Traumatic Brain Injury (TBI).
Status: Enrolling
Updated:  6/2/2012
Center for Vision Development - (Research is being conducted online)
mi
from
New Market, MD
How Well do Patients With Traumatic Brain Injury Learn New Material Using Learning Styles in Online Science Classrooms?
Instructional Design Strategies to Support Adult Patients/Students (Civilian & Military) With Traumatic Brain Injury (TBI).
Status: Enrolling
Updated: 6/2/2012
Center for Vision Development - (Research is being conducted online)
mi
from
New Market, MD
Click here to add this to my saved trials
A Prospective Study to Evaluate Use of the Tibion Bionic Leg in Sub-Acute Post-stroke Patients
A Prospective, Experimental ABA Study to Evaluate Use of the Tibion Bionic Leg in Subacute Post-stroke Patients Undergoing Physical Therapy
Status: Archived
Updated:  6/4/2012
Magee Rehabilitation Hospital
mi
from
Philadelphia, PA
A Prospective Study to Evaluate Use of the Tibion Bionic Leg in Sub-Acute Post-stroke Patients
A Prospective, Experimental ABA Study to Evaluate Use of the Tibion Bionic Leg in Subacute Post-stroke Patients Undergoing Physical Therapy
Status: Archived
Updated: 6/4/2012
Magee Rehabilitation Hospital
mi
from
Philadelphia, PA
Treating Acutely Agitated Patients With Asenapine Sublingual Tablets
Treating Acutely Agitated Patients With Asenapine Sublingual Tablets: A Single-Dose, Randomized, Double-Blind Placebo Controlled Trial
Status: Enrolling
Updated:  6/5/2012
St. Joseph's Hospital Health Center-Comprehensive Psychiatric Emergency Program (CPEP)
mi
from
Syracuse, NY
Treating Acutely Agitated Patients With Asenapine Sublingual Tablets
Treating Acutely Agitated Patients With Asenapine Sublingual Tablets: A Single-Dose, Randomized, Double-Blind Placebo Controlled Trial
Status: Enrolling
Updated: 6/5/2012
St. Joseph's Hospital Health Center-Comprehensive Psychiatric Emergency Program (CPEP)
mi
from
Syracuse, NY
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3-Dimensional Accelerometer Sub-Study
3-Dimensional Accelerometer Sub-Study for Patients Participating in the E-30 Study: Heart Rate Changes in Subjects With Epilepsy During an Epilepsy Monitoring Unit Admission
Status: Enrolling
Updated:  6/5/2012
Clinical Research Facility
mi
from
Daytona Beach, FL
3-Dimensional Accelerometer Sub-Study
3-Dimensional Accelerometer Sub-Study for Patients Participating in the E-30 Study: Heart Rate Changes in Subjects With Epilepsy During an Epilepsy Monitoring Unit Admission
Status: Enrolling
Updated: 6/5/2012
Clinical Research Facility
mi
from
Daytona Beach, FL
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3-Dimensional Accelerometer Sub-Study
3-Dimensional Accelerometer Sub-Study for Patients Participating in the E-30 Study: Heart Rate Changes in Subjects With Epilepsy During an Epilepsy Monitoring Unit Admission
Status: Enrolling
Updated:  6/5/2012
Clinical Research Facility
mi
from
Park Ridge, IL
3-Dimensional Accelerometer Sub-Study
3-Dimensional Accelerometer Sub-Study for Patients Participating in the E-30 Study: Heart Rate Changes in Subjects With Epilepsy During an Epilepsy Monitoring Unit Admission
Status: Enrolling
Updated: 6/5/2012
Clinical Research Facility
mi
from
Park Ridge, IL
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The Effects of Mindfulness Based Stress Reduction on Patients With Traumatic Brain Injury
The Effects of Mindfulness Based Stress Reduction on Patients With Traumatic Brain Injury
Status: Enrolling
Updated:  6/5/2012
Spaulding Rehabilitation Hospital
mi
from
Boston, MA
The Effects of Mindfulness Based Stress Reduction on Patients With Traumatic Brain Injury
The Effects of Mindfulness Based Stress Reduction on Patients With Traumatic Brain Injury
Status: Enrolling
Updated: 6/5/2012
Spaulding Rehabilitation Hospital
mi
from
Boston, MA
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Diagnostic Utility of MRI in Intracerebral Hemorrhage
Diagnostic Utility of MRI in Intracerebral Hemorrhage
Status: Enrolling
Updated:  6/12/2012
Stanford University School of Medicine
mi
from
Stanford, CA
Diagnostic Utility of MRI in Intracerebral Hemorrhage
Diagnostic Utility of MRI in Intracerebral Hemorrhage
Status: Enrolling
Updated: 6/12/2012
Stanford University School of Medicine
mi
from
Stanford, CA
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Arm Rehabilitation Study After Stroke
Interdisciplinary Comprehensive Arm Rehab Evaluation (ICARE) Stroke Initiative
Status: Enrolling
Updated:  6/12/2012
University of Southern California
mi
from
Los Angeles, CA
Arm Rehabilitation Study After Stroke
Interdisciplinary Comprehensive Arm Rehab Evaluation (ICARE) Stroke Initiative
Status: Enrolling
Updated: 6/12/2012
University of Southern California
mi
from
Los Angeles, CA
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Arm Rehabilitation Study After Stroke
Interdisciplinary Comprehensive Arm Rehab Evaluation (ICARE) Stroke Initiative
Status: Enrolling
Updated:  6/12/2012
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
Arm Rehabilitation Study After Stroke
Interdisciplinary Comprehensive Arm Rehab Evaluation (ICARE) Stroke Initiative
Status: Enrolling
Updated: 6/12/2012
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
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Arm Rehabilitation Study After Stroke
Interdisciplinary Comprehensive Arm Rehab Evaluation (ICARE) Stroke Initiative
Status: Enrolling
Updated:  6/12/2012
Rancho Los Amigos National Rehabilitation Center
mi
from
Los Angeles (Downey), CA
Arm Rehabilitation Study After Stroke
Interdisciplinary Comprehensive Arm Rehab Evaluation (ICARE) Stroke Initiative
Status: Enrolling
Updated: 6/12/2012
Rancho Los Amigos National Rehabilitation Center
mi
from
Los Angeles (Downey), CA
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Arm Rehabilitation Study After Stroke
Interdisciplinary Comprehensive Arm Rehab Evaluation (ICARE) Stroke Initiative
Status: Enrolling
Updated:  6/12/2012
Long Beach Memorial Medical Center
mi
from
Long Beach, CA
Arm Rehabilitation Study After Stroke
Interdisciplinary Comprehensive Arm Rehab Evaluation (ICARE) Stroke Initiative
Status: Enrolling
Updated: 6/12/2012
Long Beach Memorial Medical Center
mi
from
Long Beach, CA
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Arm Rehabilitation Study After Stroke
Interdisciplinary Comprehensive Arm Rehab Evaluation (ICARE) Stroke Initiative
Status: Enrolling
Updated:  6/12/2012
Huntington Rehabilitation Medicine Associates
mi
from
Los Angeles (Pasadena), CA
Arm Rehabilitation Study After Stroke
Interdisciplinary Comprehensive Arm Rehab Evaluation (ICARE) Stroke Initiative
Status: Enrolling
Updated: 6/12/2012
Huntington Rehabilitation Medicine Associates
mi
from
Los Angeles (Pasadena), CA
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