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

Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: Enrolling
Updated:  2/2/2018
SPARC Site 73
mi
from
Eugene, OR
Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: Enrolling
Updated: 2/2/2018
SPARC Site 73
mi
from
Eugene, OR
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Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: Enrolling
Updated:  2/2/2018
SPARC Site 91
mi
from
Dresden,
Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: Enrolling
Updated: 2/2/2018
SPARC Site 91
mi
from
Dresden,
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Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: Enrolling
Updated:  2/2/2018
SPARC Site 8
mi
from
Washington,
Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: Enrolling
Updated: 2/2/2018
SPARC Site 8
mi
from
Washington,
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Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: Enrolling
Updated:  2/2/2018
SPARC Site 28
mi
from
Foxboro, MA
Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: Enrolling
Updated: 2/2/2018
SPARC Site 28
mi
from
Foxboro, MA
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Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: Enrolling
Updated:  2/2/2018
SPARC Site 30
mi
from
Clinton Township, MI
Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: Enrolling
Updated: 2/2/2018
SPARC Site 30
mi
from
Clinton Township, MI
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Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: Enrolling
Updated:  2/2/2018
SPARC Site 74
mi
from
Henderson, NV
Efficacy and Safety of SPARC0921 in Subjects With Spasticity
Status: Enrolling
Updated: 2/2/2018
SPARC Site 74
mi
from
Henderson, NV
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The General Use of Robots in Stroke Recovery
Pilot Study of the Effects of Protocol-Specific Robotic Arm Therapy in Stroke Recovery
Status: Enrolling
Updated:  2/2/2018
The Feinstein Institute for Medical Research
mi
from
Manhasset, NY
The General Use of Robots in Stroke Recovery
Pilot Study of the Effects of Protocol-Specific Robotic Arm Therapy in Stroke Recovery
Status: Enrolling
Updated: 2/2/2018
The Feinstein Institute for Medical Research
mi
from
Manhasset, NY
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Imaging Dopamine Function and Its Impact on Outcome After Traumatic Brain Injury (TBI)
Imaging Dopamine Function and Its Impact on Outcome After Traumatic Brain Injury (TBI)
Status: Enrolling
Updated:  2/2/2018
Baylor Research Institute
mi
from
Dallas, TX
Imaging Dopamine Function and Its Impact on Outcome After Traumatic Brain Injury (TBI)
Imaging Dopamine Function and Its Impact on Outcome After Traumatic Brain Injury (TBI)
Status: Enrolling
Updated: 2/2/2018
Baylor Research Institute
mi
from
Dallas, TX
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Gene Transfer Clinical Trial for Duchenne Muscular Dystrophy Using rAAVrh74.MCK.GALGT2
Phase I Gene Transfer Clinical Trial for Duchenne Muscular Dystrophy Using rAAVrh74.MCK.GALGT2
Status: Enrolling
Updated:  2/2/2018
Nationwide Children's Hospital
mi
from
Columbus, OH
Gene Transfer Clinical Trial for Duchenne Muscular Dystrophy Using rAAVrh74.MCK.GALGT2
Phase I Gene Transfer Clinical Trial for Duchenne Muscular Dystrophy Using rAAVrh74.MCK.GALGT2
Status: Enrolling
Updated: 2/2/2018
Nationwide Children's Hospital
mi
from
Columbus, OH
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Cooling to Optimize Organ Life in Donor Study
Feasibility of Mild-to-moderate Therapeutic Hypothermia as an In-vivo Organ Preservation Strategy in Brain-dead Donors
Status: Enrolling
Updated:  2/5/2018
University of Pittsburgh Medical Center
mi
from
Pittsburgh, PA
Cooling to Optimize Organ Life in Donor Study
Feasibility of Mild-to-moderate Therapeutic Hypothermia as an In-vivo Organ Preservation Strategy in Brain-dead Donors
Status: Enrolling
Updated: 2/5/2018
University of Pittsburgh Medical Center
mi
from
Pittsburgh, PA
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Virtual Reality (VR) Treatment for Balance Problems in Traumatic Brain Injury (TBI)
Home-Based Virtual Reality (VR) Treatment for Chronic Balance Problems in Adults With Traumatic Brain Injury
Status: Enrolling
Updated:  2/5/2018
Craig Hospital
mi
from
Englewood, CO
Virtual Reality (VR) Treatment for Balance Problems in Traumatic Brain Injury (TBI)
Home-Based Virtual Reality (VR) Treatment for Chronic Balance Problems in Adults With Traumatic Brain Injury
Status: Enrolling
Updated: 2/5/2018
Craig Hospital
mi
from
Englewood, CO
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Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US015
mi
from
Beverly Hills, CA
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US015
mi
from
Beverly Hills, CA
Click here to add this to my saved trials
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US002
mi
from
Garden Grove, CA
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US002
mi
from
Garden Grove, CA
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Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US004
mi
from
National City, CA
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US004
mi
from
National City, CA
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Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US013
mi
from
Bradenton, FL
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US013
mi
from
Bradenton, FL
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Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US006
mi
from
Gainesville, FL
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US006
mi
from
Gainesville, FL
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Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US010
mi
from
Alpharetta, GA
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US010
mi
from
Alpharetta, GA
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Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US014
mi
from
Libertyville, IL
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US014
mi
from
Libertyville, IL
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Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US011
mi
from
Baltimore, MD
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US011
mi
from
Baltimore, MD
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Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US009
mi
from
Boston, MA
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US009
mi
from
Boston, MA
Click here to add this to my saved trials
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US005
mi
from
New York, NY
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US005
mi
from
New York, NY
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Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US008
mi
from
New York, NY
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US008
mi
from
New York, NY
Click here to add this to my saved trials
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US001
mi
from
Austin, TX
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US001
mi
from
Austin, TX
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Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US007
mi
from
Herndon, VA
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US007
mi
from
Herndon, VA
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Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US003
mi
from
Bellevue, WA
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US003
mi
from
Bellevue, WA
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Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated:  2/5/2018
US016
mi
from
Las Vegas, NV
Investigating the Effect of Vortioxetine in Adult ADHD Patients
Interventional, Randomised, Double-blind, Placebo-controlled, Fixed-dose Study of Vortioxetine in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
Status: Enrolling
Updated: 2/5/2018
US016
mi
from
Las Vegas, NV
Click here to add this to my saved trials
Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated:  2/5/2018
Consultans in Epilepsy & Neurology, PLLC
mi
from
Boise, ID
Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated: 2/5/2018
Consultans in Epilepsy & Neurology, PLLC
mi
from
Boise, ID
Click here to add this to my saved trials
Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated:  2/5/2018
Bluegrass Epilepsy Research
mi
from
Lexington, KY
Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated: 2/5/2018
Bluegrass Epilepsy Research
mi
from
Lexington, KY
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Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated:  2/5/2018
Mid-Atlantic Epilepsy Center
mi
from
Bethesda, MD
Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated: 2/5/2018
Mid-Atlantic Epilepsy Center
mi
from
Bethesda, MD
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Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated:  2/5/2018
Minneapolis Clinic of Neurology
mi
from
Golden Valley, MN
Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated: 2/5/2018
Minneapolis Clinic of Neurology
mi
from
Golden Valley, MN
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Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated:  2/5/2018
Clinilabs Inc.
mi
from
New York, NY
Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated: 2/5/2018
Clinilabs Inc.
mi
from
New York, NY
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Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated:  2/5/2018
NeurologicalClinic of Texas, P.A.
mi
from
Dallas, TX
Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated: 2/5/2018
NeurologicalClinic of Texas, P.A.
mi
from
Dallas, TX
Click here to add this to my saved trials
Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated:  2/5/2018
The More foundation/The Core Institute
mi
from
Sun City, AZ
Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements for Subjects Treated With Eslicarbazeine Acetate (ESL)
Ex-vivo Study to Evaluate Serum Free Thyroxine (FT4) and Free Triiodothyronine (FT3) Measurements Using Equilibrium Dialysis (ED) and Automated Kit Assay for Subjects Treated With Eslicarbazeine Acetate
Status: Enrolling
Updated: 2/5/2018
The More foundation/The Core Institute
mi
from
Sun City, AZ
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Genetic and Environmental Risk Factors for Hemorrhagic Stroke-GERFHS III
Genetic and Environmental Risk Factors for Hemorrhagic Stroke
Status: Enrolling
Updated:  2/5/2018
University of Cincinnati Department of Neurology
mi
from
Cincinnati, OH
Genetic and Environmental Risk Factors for Hemorrhagic Stroke-GERFHS III
Genetic and Environmental Risk Factors for Hemorrhagic Stroke
Status: Enrolling
Updated: 2/5/2018
University of Cincinnati Department of Neurology
mi
from
Cincinnati, OH
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Using Web-based Technology to Expand and Enhance Applied Behavioral Analysis Programs for Children With Autism in Military Families
Using Technology to Expand and Enhance Applied Behavioral Analysis Programs for Children With Autism in Military Families
Status: Enrolling
Updated:  2/6/2018
Univ of Nebraska Med Ctr
mi
from
Omaha, NE
Using Web-based Technology to Expand and Enhance Applied Behavioral Analysis Programs for Children With Autism in Military Families
Using Technology to Expand and Enhance Applied Behavioral Analysis Programs for Children With Autism in Military Families
Status: Enrolling
Updated: 2/6/2018
Univ of Nebraska Med Ctr
mi
from
Omaha, NE
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Outcome Evaluation of Ceramic Crowns Using Two Different Dental Cements
Outcome Evaluation of All Ceramic Crowns and Fixed Partial Dentures Bonded With Two Different Dental Cements.
Status: Enrolling
Updated:  2/6/2018
University of Iowa, College of Dentistry
mi
from
Iowa City, IA
Outcome Evaluation of Ceramic Crowns Using Two Different Dental Cements
Outcome Evaluation of All Ceramic Crowns and Fixed Partial Dentures Bonded With Two Different Dental Cements.
Status: Enrolling
Updated: 2/6/2018
University of Iowa, College of Dentistry
mi
from
Iowa City, IA
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Creatine Safety & Tolerability in Huntington's Disease
Creatine Safety & Tolerability in Huntington's Disease (CREST-X): A Single-Center, Open-Label, Long-Term Safety & Tolerability Extension Study of Creatine in Subjects With HD
Status: Enrolling
Updated:  2/6/2018
Massachusetts General Hospital
mi
from
Charlestown, MA
Creatine Safety & Tolerability in Huntington's Disease
Creatine Safety & Tolerability in Huntington's Disease (CREST-X): A Single-Center, Open-Label, Long-Term Safety & Tolerability Extension Study of Creatine in Subjects With HD
Status: Enrolling
Updated: 2/6/2018
Massachusetts General Hospital
mi
from
Charlestown, MA
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Somatosensory Profiling in Radicular Pain Patients And it's Correlation With Treatment Outcome
Somatosensory Profiling in Radicular Pain Patients And it's Correlation With Treatment Outcome
Status: Enrolling
Updated:  2/7/2018
MGH Center for Translational Pain Research
mi
from
Boston, MA
Somatosensory Profiling in Radicular Pain Patients And it's Correlation With Treatment Outcome
Somatosensory Profiling in Radicular Pain Patients And it's Correlation With Treatment Outcome
Status: Enrolling
Updated: 2/7/2018
MGH Center for Translational Pain Research
mi
from
Boston, MA
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REACH OUT: to Reduce High Blood Pressure in the Emergency Department
Status: Enrolling
Updated:  2/7/2018
Clinical Research Facility
mi
from
Ann Arbor, MI
REACH OUT: to Reduce High Blood Pressure in the Emergency Department
Status: Enrolling
Updated: 2/7/2018
Clinical Research Facility
mi
from
Ann Arbor, MI
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Open-label Study of Liothyronine in MS
A Phase 1b, Open-label Study to Evaluate the Safety and Tolerability of the Putative Remyelinating Agent, Liothyronine, in Individuals With MS
Status: Enrolling
Updated:  2/8/2018
Johns Hopkins Hospital
mi
from
Baltimore, MD
Open-label Study of Liothyronine in MS
A Phase 1b, Open-label Study to Evaluate the Safety and Tolerability of the Putative Remyelinating Agent, Liothyronine, in Individuals With MS
Status: Enrolling
Updated: 2/8/2018
Johns Hopkins Hospital
mi
from
Baltimore, MD
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Combination of an Investigational Cannabinoid and Methadone for HIV-associated Neuropathy
NARC 011: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study of Methadone and Combination of Methadone and SAB378 in HIV-associated Painful Peripheral Neuropathy
Status: Enrolling
Updated:  2/8/2018
University of California, San Diego
mi
from
San Diego, CA
Combination of an Investigational Cannabinoid and Methadone for HIV-associated Neuropathy
NARC 011: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study of Methadone and Combination of Methadone and SAB378 in HIV-associated Painful Peripheral Neuropathy
Status: Enrolling
Updated: 2/8/2018
University of California, San Diego
mi
from
San Diego, CA
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Combination of an Investigational Cannabinoid and Methadone for HIV-associated Neuropathy
NARC 011: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study of Methadone and Combination of Methadone and SAB378 in HIV-associated Painful Peripheral Neuropathy
Status: Enrolling
Updated:  2/8/2018
University of New York Downstate Medical Center
mi
from
Brooklyn, NY
Combination of an Investigational Cannabinoid and Methadone for HIV-associated Neuropathy
NARC 011: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study of Methadone and Combination of Methadone and SAB378 in HIV-associated Painful Peripheral Neuropathy
Status: Enrolling
Updated: 2/8/2018
University of New York Downstate Medical Center
mi
from
Brooklyn, NY
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Combination of an Investigational Cannabinoid and Methadone for HIV-associated Neuropathy
NARC 011: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study of Methadone and Combination of Methadone and SAB378 in HIV-associated Painful Peripheral Neuropathy
Status: Enrolling
Updated:  2/8/2018
University of Rochester
mi
from
Rochester, NY
Combination of an Investigational Cannabinoid and Methadone for HIV-associated Neuropathy
NARC 011: A Phase II, Randomized, Double-Blind, Placebo-Controlled Study of Methadone and Combination of Methadone and SAB378 in HIV-associated Painful Peripheral Neuropathy
Status: Enrolling
Updated: 2/8/2018
University of Rochester
mi
from
Rochester, NY
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Dopaminergic Effects on Cortical Function in Tourette's (Levodopa Protocol)
Dopaminergic Effects on Cortical Function in Tourette's (Levodopa Protocol)
Status: Enrolling
Updated:  2/8/2018
Washington Universisty School of Medicine
mi
from
Saint Louis, MO
Dopaminergic Effects on Cortical Function in Tourette's (Levodopa Protocol)
Dopaminergic Effects on Cortical Function in Tourette's (Levodopa Protocol)
Status: Enrolling
Updated: 2/8/2018
Washington Universisty School of Medicine
mi
from
Saint Louis, MO
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Detecting Dopaminergic Deficits in Individuals At-risk for Parkinsonism
Detecting Dopaminergic Deficits in Individuals At-risk for Parkinsonism
Status: Enrolling
Updated:  2/9/2018
University of Minnesota, Center for Magnetic Resonance Research
mi
from
Minneapolis, MN
Detecting Dopaminergic Deficits in Individuals At-risk for Parkinsonism
Detecting Dopaminergic Deficits in Individuals At-risk for Parkinsonism
Status: Enrolling
Updated: 2/9/2018
University of Minnesota, Center for Magnetic Resonance Research
mi
from
Minneapolis, MN
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Intensive Versus Standard Blood Pressure Lowering to Prevent Functional Decline in Older People
Intensive Versus Standard Blood Pressure Lowering to Prevent Functional Decline in Older People
Status: Enrolling
Updated:  2/9/2018
University of Connecticut Health Center
mi
from
Farmington, CT
Intensive Versus Standard Blood Pressure Lowering to Prevent Functional Decline in Older People
Intensive Versus Standard Blood Pressure Lowering to Prevent Functional Decline in Older People
Status: Enrolling
Updated: 2/9/2018
University of Connecticut Health Center
mi
from
Farmington, CT
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LARGE Aneurysm Randomized Trial: Flow Diversion Versus Traditional Endovascular Coiling Therapy
LARGE Aneurysm Randomized Trial: Flow Diversion Versus Traditional Endovascular Coiling Therapy
Status: Enrolling
Updated:  2/9/2018
MUSC
mi
from
Charleston, SC
LARGE Aneurysm Randomized Trial: Flow Diversion Versus Traditional Endovascular Coiling Therapy
LARGE Aneurysm Randomized Trial: Flow Diversion Versus Traditional Endovascular Coiling Therapy
Status: Enrolling
Updated: 2/9/2018
MUSC
mi
from
Charleston, SC
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COMPASS Trial: a Direct Aspiration First Pass Technique
COMPASS Trial: a Direct Aspiration First Pass Technique
Status: Enrolling
Updated:  2/9/2018
Medical University of South Carolina
mi
from
Charleston, SC
COMPASS Trial: a Direct Aspiration First Pass Technique
COMPASS Trial: a Direct Aspiration First Pass Technique
Status: Enrolling
Updated: 2/9/2018
Medical University of South Carolina
mi
from
Charleston, SC
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Safety and Tolerability of PF-05230907 in Intracerebral Hemorrhage
A Phase 1b Multicenter, Open-label Study To Evaluate The Safety And Tolerability And Determine The Maximum Tolerated Dose Of Pf-05230907 In Subjects With Intracerebral Hemorrhage (Ich)
Status: Enrolling
Updated:  2/9/2018
The James Cancer Hospital and Solove Research Institute
mi
from
Columbus, OH
Safety and Tolerability of PF-05230907 in Intracerebral Hemorrhage
A Phase 1b Multicenter, Open-label Study To Evaluate The Safety And Tolerability And Determine The Maximum Tolerated Dose Of Pf-05230907 In Subjects With Intracerebral Hemorrhage (Ich)
Status: Enrolling
Updated: 2/9/2018
The James Cancer Hospital and Solove Research Institute
mi
from
Columbus, OH
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Safety and Tolerability of PF-05230907 in Intracerebral Hemorrhage
A Phase 1b Multicenter, Open-label Study To Evaluate The Safety And Tolerability And Determine The Maximum Tolerated Dose Of Pf-05230907 In Subjects With Intracerebral Hemorrhage (Ich)
Status: Enrolling
Updated:  2/9/2018
The Ohio State University, Wexner Medical Center
mi
from
Columbus, OH
Safety and Tolerability of PF-05230907 in Intracerebral Hemorrhage
A Phase 1b Multicenter, Open-label Study To Evaluate The Safety And Tolerability And Determine The Maximum Tolerated Dose Of Pf-05230907 In Subjects With Intracerebral Hemorrhage (Ich)
Status: Enrolling
Updated: 2/9/2018
The Ohio State University, Wexner Medical Center
mi
from
Columbus, OH
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