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

A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated:  12/31/1969
Cincinnati Children's Hospital Medical Center
mi
from
Cincinnati, OH
A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated: 12/31/1969
Cincinnati Children's Hospital Medical Center
mi
from
Cincinnati, OH
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A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated:  12/31/1969
University of Iowa Stead Family Children's Hospital
mi
from
Iowa City, IA
A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated: 12/31/1969
University of Iowa Stead Family Children's Hospital
mi
from
Iowa City, IA
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A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated:  12/31/1969
Children's Hospital of Wisconsin
mi
from
Milwaukee, WI
A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated: 12/31/1969
Children's Hospital of Wisconsin
mi
from
Milwaukee, WI
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A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated:  12/31/1969
Children's/ UT Southwestern Medical Center
mi
from
Dallas, TX
A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated: 12/31/1969
Children's/ UT Southwestern Medical Center
mi
from
Dallas, TX
Click here to add this to my saved trials
A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated:  12/31/1969
University of Massachusetts Medical Center
mi
from
Worcester, MA
A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated: 12/31/1969
University of Massachusetts Medical Center
mi
from
Worcester, MA
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A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated:  12/31/1969
Ronald Reagan UCLA Medical Center
mi
from
Los Angeles, CA
A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated: 12/31/1969
Ronald Reagan UCLA Medical Center
mi
from
Los Angeles, CA
Click here to add this to my saved trials
A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated:  12/31/1969
Virginia Commonwealth University
mi
from
Richmond, VA
A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of Intravenous Delivery of Allogeneic Cardiosphere-Derived Cells in Subjects With Duchenne Muscular Dystrophy
Status: Enrolling
Updated: 12/31/1969
Virginia Commonwealth University
mi
from
Richmond, VA
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Flibanserin (Addyi®) vs. Flibanserin and Sex Therapy
Two Arm Open Label Pilot Study of Flibanserin (Addyi®) vs. Flibanserin and Sex Therapy
Status: Enrolling
Updated:  12/31/1969
San Diego Sexual Medicine
mi
from
San Diego, CA
Flibanserin (Addyi®) vs. Flibanserin and Sex Therapy
Two Arm Open Label Pilot Study of Flibanserin (Addyi®) vs. Flibanserin and Sex Therapy
Status: Enrolling
Updated: 12/31/1969
San Diego Sexual Medicine
mi
from
San Diego, CA
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Safety and Tolerability of WVE-210201 in Patients With Duchenne Muscular Dystrophy
A Multicenter, Double-blind, Placebo-controlled, Phase 1 Study of WVE-210201 Administered Intravenously to Patients With Duchenne Muscular Dystrophy
Status: Enrolling
Updated:  12/31/1969
Rare Disease Research, LLC
mi
from
Atlanta, GA
Safety and Tolerability of WVE-210201 in Patients With Duchenne Muscular Dystrophy
A Multicenter, Double-blind, Placebo-controlled, Phase 1 Study of WVE-210201 Administered Intravenously to Patients With Duchenne Muscular Dystrophy
Status: Enrolling
Updated: 12/31/1969
Rare Disease Research, LLC
mi
from
Atlanta, GA
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Safety and Tolerability of WVE-210201 in Patients With Duchenne Muscular Dystrophy
A Multicenter, Double-blind, Placebo-controlled, Phase 1 Study of WVE-210201 Administered Intravenously to Patients With Duchenne Muscular Dystrophy
Status: Enrolling
Updated:  12/31/1969
UZ Gent
mi
from
Gent,
Safety and Tolerability of WVE-210201 in Patients With Duchenne Muscular Dystrophy
A Multicenter, Double-blind, Placebo-controlled, Phase 1 Study of WVE-210201 Administered Intravenously to Patients With Duchenne Muscular Dystrophy
Status: Enrolling
Updated: 12/31/1969
UZ Gent
mi
from
Gent,
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Randomized Evaluation of Ten Allergy Skin Prick Test Devices
Randomized Evaluation of Ten Allergy Skin Prick Test Devices
Status: Enrolling
Updated:  12/31/1969
John Hopkins Asthma and Allergy Center
mi
from
Baltimore, MD
Randomized Evaluation of Ten Allergy Skin Prick Test Devices
Randomized Evaluation of Ten Allergy Skin Prick Test Devices
Status: Enrolling
Updated: 12/31/1969
John Hopkins Asthma and Allergy Center
mi
from
Baltimore, MD
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Mechanisms of Walking Recovery After Stroke
Mechanisms of Walking Recovery After Stroke
Status: Enrolling
Updated:  12/31/1969
University of Cincinnati
mi
from
Cincinnati, OH
Mechanisms of Walking Recovery After Stroke
Mechanisms of Walking Recovery After Stroke
Status: Enrolling
Updated: 12/31/1969
University of Cincinnati
mi
from
Cincinnati, OH
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Monitoring of Multiple Sclerosis (MS) Participants With the Use of Digital Technology (Smartphones and Smartwatches) - A Feasibility Study
Status: Enrolling
Updated:  12/31/1969
UCSF- Multiple Sclerosis Centre; Department of Neurology
mi
from
San Francisco, CA
Monitoring of Multiple Sclerosis (MS) Participants With the Use of Digital Technology (Smartphones and Smartwatches) - A Feasibility Study
Status: Enrolling
Updated: 12/31/1969
UCSF- Multiple Sclerosis Centre; Department of Neurology
mi
from
San Francisco, CA
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Monitoring of Multiple Sclerosis (MS) Participants With the Use of Digital Technology (Smartphones and Smartwatches) - A Feasibility Study
Status: Enrolling
Updated:  12/31/1969
Hospital Vall d'Hebron; Servicio de Neurología
mi
from
Barcelona,
Monitoring of Multiple Sclerosis (MS) Participants With the Use of Digital Technology (Smartphones and Smartwatches) - A Feasibility Study
Status: Enrolling
Updated: 12/31/1969
Hospital Vall d'Hebron; Servicio de Neurología
mi
from
Barcelona,
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Learning Enhancement Through Neurostimulation in Autism
Learning Enhancement Through Neurostimulation in Autism
Status: Enrolling
Updated:  12/31/1969
Medical Univeristy of South Carolina
mi
from
Charleston, SC
Learning Enhancement Through Neurostimulation in Autism
Learning Enhancement Through Neurostimulation in Autism
Status: Enrolling
Updated: 12/31/1969
Medical Univeristy of South Carolina
mi
from
Charleston, SC
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Safety and Efficacy of Fenofibrate as a Treatment for Huntington's Disease
A Phase IIa, Randomized, Double-blind, Placebo-controlled Study of the Safety and Efficacy of Fenofibrate as a Treatment for Huntington's Disease
Status: Enrolling
Updated:  12/31/1969
University of California, Irvine
mi
from
Irvine, CA
Safety and Efficacy of Fenofibrate as a Treatment for Huntington's Disease
A Phase IIa, Randomized, Double-blind, Placebo-controlled Study of the Safety and Efficacy of Fenofibrate as a Treatment for Huntington's Disease
Status: Enrolling
Updated: 12/31/1969
University of California, Irvine
mi
from
Irvine, CA
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IRF-PAI Functional Outcomes Data(With FIM Instrument Variables)
IRF-PAI Functional Outcomes Data(With FIM Instrument Variables)
Status: Enrolling
Updated:  12/31/1969
UDSMR
mi
from
Buffalo, NY
IRF-PAI Functional Outcomes Data(With FIM Instrument Variables)
IRF-PAI Functional Outcomes Data(With FIM Instrument Variables)
Status: Enrolling
Updated: 12/31/1969
UDSMR
mi
from
Buffalo, NY
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Reduction and Prevention of Seizure Occurrence From Exposure to Auditory Stimulation in Individuals With Neurological Handicaps
Reduction and Prevention of Seizure Occurrence From Exposure to Auditory Stimulation in Individuals With Neurological Handicaps
Status: Enrolling
Updated:  12/31/1969
Medical University of South Carolina
mi
from
Charleston, SC
Reduction and Prevention of Seizure Occurrence From Exposure to Auditory Stimulation in Individuals With Neurological Handicaps
Reduction and Prevention of Seizure Occurrence From Exposure to Auditory Stimulation in Individuals With Neurological Handicaps
Status: Enrolling
Updated: 12/31/1969
Medical University of South Carolina
mi
from
Charleston, SC
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Effect of Soccer Head Gear to Reduce Concussions
The Effectiveness of Soccer Headgear to Reduce Concussion in Adolescents
Status: Enrolling
Updated:  12/31/1969
University of Wisconsin
mi
from
Madison, WI
Effect of Soccer Head Gear to Reduce Concussions
The Effectiveness of Soccer Headgear to Reduce Concussion in Adolescents
Status: Enrolling
Updated: 12/31/1969
University of Wisconsin
mi
from
Madison, WI
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Characterization of Epilepsy Patients BEEP 2b
Characterization of Epilepsy Patients At-risk for Adverse Outcomes Related to Switching Antiepileptic Drug Products: BEEP 2b Study
Status: Enrolling
Updated:  12/31/1969
University of Maryland, Baltimore
mi
from
Baltimore, MD
Characterization of Epilepsy Patients BEEP 2b
Characterization of Epilepsy Patients At-risk for Adverse Outcomes Related to Switching Antiepileptic Drug Products: BEEP 2b Study
Status: Enrolling
Updated: 12/31/1969
University of Maryland, Baltimore
mi
from
Baltimore, MD
Click here to add this to my saved trials
Efficacy Study of the LARA Wheelchair System for Subacute Stroke Patients
Lever Actuated Rehabilitation of the Arm Using Wheelchair Propulsion and Computer Gaming
Status: Enrolling
Updated:  12/31/1969
University of California, Irvine
mi
from
Irvine, CA
Efficacy Study of the LARA Wheelchair System for Subacute Stroke Patients
Lever Actuated Rehabilitation of the Arm Using Wheelchair Propulsion and Computer Gaming
Status: Enrolling
Updated: 12/31/1969
University of California, Irvine
mi
from
Irvine, CA
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Facebook for Social Skills Training in Autism: Project Rex Connect
Project Rex Connect: The Utilization of an Online Social Network by an Interprofessional Team to Aid in Skill Acquisition for Patients With Autism Spectrum Disorders
Status: Enrolling
Updated:  12/31/1969
Medical University of South Carolina
mi
from
Charleston, SC
Facebook for Social Skills Training in Autism: Project Rex Connect
Project Rex Connect: The Utilization of an Online Social Network by an Interprofessional Team to Aid in Skill Acquisition for Patients With Autism Spectrum Disorders
Status: Enrolling
Updated: 12/31/1969
Medical University of South Carolina
mi
from
Charleston, SC
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TMS for Adults With Autism and Depression
Transcranial Magnetic Stimulation for Adults With Autism Spectrum Disorder and Depression
Status: Enrolling
Updated:  12/31/1969
Medical University of South Carolina
mi
from
Charleston, SC
TMS for Adults With Autism and Depression
Transcranial Magnetic Stimulation for Adults With Autism Spectrum Disorder and Depression
Status: Enrolling
Updated: 12/31/1969
Medical University of South Carolina
mi
from
Charleston, SC
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Open-label Study to Evaluate Safety, Tolerability and PK of BHV-0223 in ALS
Open-Label Study to Evaluate Safety, Tolerability and Pharmacokinetics of Multiple Doses of BHV-0223 in Subjects With Amyotrophic Lateral Sclerosis
Status: Enrolling
Updated:  12/31/1969
Holy Cross Neuroscience Research Institute
mi
from
Fort Lauderdale, FL
Open-label Study to Evaluate Safety, Tolerability and PK of BHV-0223 in ALS
Open-Label Study to Evaluate Safety, Tolerability and Pharmacokinetics of Multiple Doses of BHV-0223 in Subjects With Amyotrophic Lateral Sclerosis
Status: Enrolling
Updated: 12/31/1969
Holy Cross Neuroscience Research Institute
mi
from
Fort Lauderdale, FL
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Open-label Study to Evaluate Safety, Tolerability and PK of BHV-0223 in ALS
Open-Label Study to Evaluate Safety, Tolerability and Pharmacokinetics of Multiple Doses of BHV-0223 in Subjects With Amyotrophic Lateral Sclerosis
Status: Enrolling
Updated:  12/31/1969
Somnos/Neurology Associates Clinical Research
mi
from
Lincoln, NE
Open-label Study to Evaluate Safety, Tolerability and PK of BHV-0223 in ALS
Open-Label Study to Evaluate Safety, Tolerability and Pharmacokinetics of Multiple Doses of BHV-0223 in Subjects With Amyotrophic Lateral Sclerosis
Status: Enrolling
Updated: 12/31/1969
Somnos/Neurology Associates Clinical Research
mi
from
Lincoln, NE
Click here to add this to my saved trials
Open-label Study to Evaluate Safety, Tolerability and PK of BHV-0223 in ALS
Open-Label Study to Evaluate Safety, Tolerability and Pharmacokinetics of Multiple Doses of BHV-0223 in Subjects With Amyotrophic Lateral Sclerosis
Status: Enrolling
Updated:  12/31/1969
Neurosciences Institute: Neurology - Charlotte
mi
from
Charlotte, NC
Open-label Study to Evaluate Safety, Tolerability and PK of BHV-0223 in ALS
Open-Label Study to Evaluate Safety, Tolerability and Pharmacokinetics of Multiple Doses of BHV-0223 in Subjects With Amyotrophic Lateral Sclerosis
Status: Enrolling
Updated: 12/31/1969
Neurosciences Institute: Neurology - Charlotte
mi
from
Charlotte, NC
Click here to add this to my saved trials
Open-label Study to Evaluate Safety, Tolerability and PK of BHV-0223 in ALS
Open-Label Study to Evaluate Safety, Tolerability and Pharmacokinetics of Multiple Doses of BHV-0223 in Subjects With Amyotrophic Lateral Sclerosis
Status: Enrolling
Updated:  12/31/1969
Wesley Neurology Clinic
mi
from
Cordova, TN
Open-label Study to Evaluate Safety, Tolerability and PK of BHV-0223 in ALS
Open-Label Study to Evaluate Safety, Tolerability and Pharmacokinetics of Multiple Doses of BHV-0223 in Subjects With Amyotrophic Lateral Sclerosis
Status: Enrolling
Updated: 12/31/1969
Wesley Neurology Clinic
mi
from
Cordova, TN
Click here to add this to my saved trials
Open-label Study to Evaluate Safety, Tolerability and PK of BHV-0223 in ALS
Open-Label Study to Evaluate Safety, Tolerability and Pharmacokinetics of Multiple Doses of BHV-0223 in Subjects With Amyotrophic Lateral Sclerosis
Status: Enrolling
Updated:  12/31/1969
Texas Neurology, PA
mi
from
Dallas, TX
Open-label Study to Evaluate Safety, Tolerability and PK of BHV-0223 in ALS
Open-Label Study to Evaluate Safety, Tolerability and Pharmacokinetics of Multiple Doses of BHV-0223 in Subjects With Amyotrophic Lateral Sclerosis
Status: Enrolling
Updated: 12/31/1969
Texas Neurology, PA
mi
from
Dallas, TX
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Beta Blockade in in Traumatic Brain Injury
Beta-Adrenergic Blockade for Suppression of Catecholamine Surge Following Traumatic Brain Injury: A Randomized Trial
Status: Enrolling
Updated:  12/31/1969
Regional One Health
mi
from
Memphis, TN
Beta Blockade in in Traumatic Brain Injury
Beta-Adrenergic Blockade for Suppression of Catecholamine Surge Following Traumatic Brain Injury: A Randomized Trial
Status: Enrolling
Updated: 12/31/1969
Regional One Health
mi
from
Memphis, TN
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Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (PSP) Who Completed Study C2N-8E12-WW-104
Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (PSP) Who Completed Study C2N-8E12-WW-104
Status: Enrolling
Updated:  12/31/1969
University of California, San Diego /ID# 170113
mi
from
La Jolla, CA
Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (PSP) Who Completed Study C2N-8E12-WW-104
Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (PSP) Who Completed Study C2N-8E12-WW-104
Status: Enrolling
Updated: 12/31/1969
University of California, San Diego /ID# 170113
mi
from
La Jolla, CA
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Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (PSP) Who Completed Study C2N-8E12-WW-104
Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (PSP) Who Completed Study C2N-8E12-WW-104
Status: Enrolling
Updated:  12/31/1969
Kerwin Research Center /ID# 170112
mi
from
Dallas, TX
Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (PSP) Who Completed Study C2N-8E12-WW-104
Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (PSP) Who Completed Study C2N-8E12-WW-104
Status: Enrolling
Updated: 12/31/1969
Kerwin Research Center /ID# 170112
mi
from
Dallas, TX
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A Pilot Study of Creative Arts Interventions for Neurology Inpatients
A Pilot Study of Creative Arts Interventions for Neurology Inpatients in the Epilepsy Monitoring Unit and the Headache Service
Status: Enrolling
Updated:  12/31/1969
Dartmouth Hitchcock Medical Center
mi
from
Lebanon, NH
A Pilot Study of Creative Arts Interventions for Neurology Inpatients
A Pilot Study of Creative Arts Interventions for Neurology Inpatients in the Epilepsy Monitoring Unit and the Headache Service
Status: Enrolling
Updated: 12/31/1969
Dartmouth Hitchcock Medical Center
mi
from
Lebanon, NH
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Anxiety and Depression in Epilepsy: A Pilot Treatment Study
Anxiety and Depression in Epilepsy: A Pilot Epileptologist-Driven Treatment Study
Status: Enrolling
Updated:  12/31/1969
Wake Forest Baptist Medical Center
mi
from
Winston-Salem, NC
Anxiety and Depression in Epilepsy: A Pilot Treatment Study
Anxiety and Depression in Epilepsy: A Pilot Epileptologist-Driven Treatment Study
Status: Enrolling
Updated: 12/31/1969
Wake Forest Baptist Medical Center
mi
from
Winston-Salem, NC
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Atomoxetine for Treating Cocaine Abuse in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Atomoxetine Treatment for Cocaine Abuse and Adult Attention-Deficit Hyperactivity Disorder (ADHD): A Preliminary Open Trial
Status: Enrolling
Updated:  12/31/1969
Research Foundation for Mental Hygiene, Inc.
mi
from
New York, NY
Atomoxetine for Treating Cocaine Abuse in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Atomoxetine Treatment for Cocaine Abuse and Adult Attention-Deficit Hyperactivity Disorder (ADHD): A Preliminary Open Trial
Status: Enrolling
Updated: 12/31/1969
Research Foundation for Mental Hygiene, Inc.
mi
from
New York, NY
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Social Skills in Children With ASD and Process Drama
Building Social Skills in Children With ASD Characteristics Through Process Drama
Status: Enrolling
Updated:  12/31/1969
University of Utah
mi
from
Salt Lake City, UT
Social Skills in Children With ASD and Process Drama
Building Social Skills in Children With ASD Characteristics Through Process Drama
Status: Enrolling
Updated: 12/31/1969
University of Utah
mi
from
Salt Lake City, UT
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Online Mindfulness-based Tic Reduction
Online Mindfulness-based Tic Reduction: Development and Testing (Phase One)
Status: Enrolling
Updated:  12/31/1969
Bowdoin College
mi
from
Brunswick, ME
Online Mindfulness-based Tic Reduction
Online Mindfulness-based Tic Reduction: Development and Testing (Phase One)
Status: Enrolling
Updated: 12/31/1969
Bowdoin College
mi
from
Brunswick, ME
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Online Mindfulness-based Tic Reduction
Online Mindfulness-based Tic Reduction: Development and Testing (Phase One)
Status: Enrolling
Updated:  12/31/1969
Massachusetts General Hospital
mi
from
Boston, MA
Online Mindfulness-based Tic Reduction
Online Mindfulness-based Tic Reduction: Development and Testing (Phase One)
Status: Enrolling
Updated: 12/31/1969
Massachusetts General Hospital
mi
from
Boston, MA
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Transcranial Magnetic Stimulation (TMS) for Primary Progressive Apraxia of Speech (PPAOS)
Investigating the Use of Transcranial Magnetic Stimulation (TMS) for Primary Progressive Apraxia of Speech (PPAOS)
Status: Enrolling
Updated:  12/31/1969
University of Miami Miller School of Medicine
mi
from
Miami, FL
Transcranial Magnetic Stimulation (TMS) for Primary Progressive Apraxia of Speech (PPAOS)
Investigating the Use of Transcranial Magnetic Stimulation (TMS) for Primary Progressive Apraxia of Speech (PPAOS)
Status: Enrolling
Updated: 12/31/1969
University of Miami Miller School of Medicine
mi
from
Miami, FL
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Safety Evaluation of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Stroke
A Multi-site, Interventional, Non-comparative, Single-arm Trial to Evaluate the Safety of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Ischemic or Hemorrhagic Stroke
Status: Enrolling
Updated:  12/31/1969
Shirley Ryan AbilityLab
mi
from
Chicago, IL
Safety Evaluation of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Stroke
A Multi-site, Interventional, Non-comparative, Single-arm Trial to Evaluate the Safety of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Ischemic or Hemorrhagic Stroke
Status: Enrolling
Updated: 12/31/1969
Shirley Ryan AbilityLab
mi
from
Chicago, IL
Click here to add this to my saved trials
Safety Evaluation of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Stroke
A Multi-site, Interventional, Non-comparative, Single-arm Trial to Evaluate the Safety of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Ischemic or Hemorrhagic Stroke
Status: Enrolling
Updated:  12/31/1969
Spaulding Rehabilitation Institute
mi
from
Boston, MA
Safety Evaluation of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Stroke
A Multi-site, Interventional, Non-comparative, Single-arm Trial to Evaluate the Safety of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Ischemic or Hemorrhagic Stroke
Status: Enrolling
Updated: 12/31/1969
Spaulding Rehabilitation Institute
mi
from
Boston, MA
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Safety Evaluation of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Stroke
A Multi-site, Interventional, Non-comparative, Single-arm Trial to Evaluate the Safety of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Ischemic or Hemorrhagic Stroke
Status: Enrolling
Updated:  12/31/1969
Kessler Foundation
mi
from
West Orange, NJ
Safety Evaluation of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Stroke
A Multi-site, Interventional, Non-comparative, Single-arm Trial to Evaluate the Safety of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Ischemic or Hemorrhagic Stroke
Status: Enrolling
Updated: 12/31/1969
Kessler Foundation
mi
from
West Orange, NJ
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Safety Evaluation of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Stroke
A Multi-site, Interventional, Non-comparative, Single-arm Trial to Evaluate the Safety of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Ischemic or Hemorrhagic Stroke
Status: Enrolling
Updated:  12/31/1969
Moss Rehab
mi
from
Elkins Park, PA
Safety Evaluation of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Stroke
A Multi-site, Interventional, Non-comparative, Single-arm Trial to Evaluate the Safety of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Ischemic or Hemorrhagic Stroke
Status: Enrolling
Updated: 12/31/1969
Moss Rehab
mi
from
Elkins Park, PA
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Safety Evaluation of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Stroke
A Multi-site, Interventional, Non-comparative, Single-arm Trial to Evaluate the Safety of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Ischemic or Hemorrhagic Stroke
Status: Enrolling
Updated:  12/31/1969
TIRR Memorial Hermann
mi
from
Houston, TX
Safety Evaluation of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Stroke
A Multi-site, Interventional, Non-comparative, Single-arm Trial to Evaluate the Safety of the ReWalk ReStore Device in Subjects With Mobility Impairments Due to Ischemic or Hemorrhagic Stroke
Status: Enrolling
Updated: 12/31/1969
TIRR Memorial Hermann
mi
from
Houston, TX
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Transcutaneous Vagus Nerve Stimulation for Motor Recovery After Stroke
Safety and Effectiveness of Transcutaneous Vagus Nerve Stimulation Therapy to Improve Motor Recovery After Stroke
Status: Enrolling
Updated:  12/31/1969
Spaulding Rehabilitation Hospital
mi
from
Boston, MA
Transcutaneous Vagus Nerve Stimulation for Motor Recovery After Stroke
Safety and Effectiveness of Transcutaneous Vagus Nerve Stimulation Therapy to Improve Motor Recovery After Stroke
Status: Enrolling
Updated: 12/31/1969
Spaulding Rehabilitation Hospital
mi
from
Boston, MA
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Game-Based Home Exercise Programs in Chronic Stroke: A Feasibility Study
Game-Based Home Exercise Programs in Chronic Stroke: A Feasibility Study
Status: Enrolling
Updated:  12/31/1969
University of Missouri
mi
from
Columbia, MO
Game-Based Home Exercise Programs in Chronic Stroke: A Feasibility Study
Game-Based Home Exercise Programs in Chronic Stroke: A Feasibility Study
Status: Enrolling
Updated: 12/31/1969
University of Missouri
mi
from
Columbia, MO
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Sensorimotor Changes in Stroke Following Mindfulness
Pilot Study of Sensorimotor Changes in Stroke Following Mindfulness
Status: Enrolling
Updated:  12/31/1969
University of Southern California
mi
from
Los Angeles, CA
Sensorimotor Changes in Stroke Following Mindfulness
Pilot Study of Sensorimotor Changes in Stroke Following Mindfulness
Status: Enrolling
Updated: 12/31/1969
University of Southern California
mi
from
Los Angeles, CA
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NOn-invasive Repeated THerapeutic STimulation for Aphasia Recovery
NOn-invasive Repeated THerapeutic STimulation for Aphasia Recovery
Status: Enrolling
Updated:  12/31/1969
Burke-Cornell Medical Research Institute
mi
from
White Plains, NY
NOn-invasive Repeated THerapeutic STimulation for Aphasia Recovery
NOn-invasive Repeated THerapeutic STimulation for Aphasia Recovery
Status: Enrolling
Updated: 12/31/1969
Burke-Cornell Medical Research Institute
mi
from
White Plains, NY
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NOn-invasive Repeated THerapeutic STimulation for Aphasia Recovery
NOn-invasive Repeated THerapeutic STimulation for Aphasia Recovery
Status: Enrolling
Updated:  12/31/1969
Sunnybrook Research Institute
mi
from
Toronto,
NOn-invasive Repeated THerapeutic STimulation for Aphasia Recovery
NOn-invasive Repeated THerapeutic STimulation for Aphasia Recovery
Status: Enrolling
Updated: 12/31/1969
Sunnybrook Research Institute
mi
from
Toronto,
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Online and Shared Decision-Making Interventions to Engage Service Men and Women in Post-Deployment Mental Health Care
Online and Shared Decision-Making Interventions to Engage Service Men and Women in Post-Deployment Mental Health Care
Status: Enrolling
Updated:  12/31/1969
Iowa City VA Health Care System, Iowa City, IA
mi
from
Iowa City, IA
Online and Shared Decision-Making Interventions to Engage Service Men and Women in Post-Deployment Mental Health Care
Online and Shared Decision-Making Interventions to Engage Service Men and Women in Post-Deployment Mental Health Care
Status: Enrolling
Updated: 12/31/1969
Iowa City VA Health Care System, Iowa City, IA
mi
from
Iowa City, IA
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Music and Adherence Home Programs Post Stroke
Music and Adherence in Upper Extremity Home Programs Post Stroke
Status: Enrolling
Updated:  12/31/1969
Duquesne University Speech, Hearing, Language Clinic
mi
from
Pittsburgh, PA
Music and Adherence Home Programs Post Stroke
Music and Adherence in Upper Extremity Home Programs Post Stroke
Status: Enrolling
Updated: 12/31/1969
Duquesne University Speech, Hearing, Language Clinic
mi
from
Pittsburgh, PA
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