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

Gabapentin in Treating Peripheral Neuropathy in Cancer Patients Undergoing Chemotherapy
The Efficacy Of Gabapentin In The Management Of Chemotherapy-Induced Peripheral Neuropathy: A Phase III Randomized, Double-Blind, Placebo-Controlled, Crossover Trial
Status: Enrolling
Updated:  7/30/2015
CCOP - Upstate Carolina
mi
from
Spartanburg, SC
Gabapentin in Treating Peripheral Neuropathy in Cancer Patients Undergoing Chemotherapy
The Efficacy Of Gabapentin In The Management Of Chemotherapy-Induced Peripheral Neuropathy: A Phase III Randomized, Double-Blind, Placebo-Controlled, Crossover Trial
Status: Enrolling
Updated: 7/30/2015
CCOP - Upstate Carolina
mi
from
Spartanburg, SC
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Gabapentin in Treating Peripheral Neuropathy in Cancer Patients Undergoing Chemotherapy
The Efficacy Of Gabapentin In The Management Of Chemotherapy-Induced Peripheral Neuropathy: A Phase III Randomized, Double-Blind, Placebo-Controlled, Crossover Trial
Status: Enrolling
Updated:  7/30/2015
Rapid City Regional Hospital
mi
from
Rapid City, SD
Gabapentin in Treating Peripheral Neuropathy in Cancer Patients Undergoing Chemotherapy
The Efficacy Of Gabapentin In The Management Of Chemotherapy-Induced Peripheral Neuropathy: A Phase III Randomized, Double-Blind, Placebo-Controlled, Crossover Trial
Status: Enrolling
Updated: 7/30/2015
Rapid City Regional Hospital
mi
from
Rapid City, SD
Click here to add this to my saved trials
Gabapentin in Treating Peripheral Neuropathy in Cancer Patients Undergoing Chemotherapy
The Efficacy Of Gabapentin In The Management Of Chemotherapy-Induced Peripheral Neuropathy: A Phase III Randomized, Double-Blind, Placebo-Controlled, Crossover Trial
Status: Enrolling
Updated:  7/30/2015
CCOP - Sioux Community Cancer Consortium
mi
from
Sioux Falls, SD
Gabapentin in Treating Peripheral Neuropathy in Cancer Patients Undergoing Chemotherapy
The Efficacy Of Gabapentin In The Management Of Chemotherapy-Induced Peripheral Neuropathy: A Phase III Randomized, Double-Blind, Placebo-Controlled, Crossover Trial
Status: Enrolling
Updated: 7/30/2015
CCOP - Sioux Community Cancer Consortium
mi
from
Sioux Falls, SD
Click here to add this to my saved trials
Gabapentin in Treating Peripheral Neuropathy in Cancer Patients Undergoing Chemotherapy
The Efficacy Of Gabapentin In The Management Of Chemotherapy-Induced Peripheral Neuropathy: A Phase III Randomized, Double-Blind, Placebo-Controlled, Crossover Trial
Status: Enrolling
Updated:  7/30/2015
CCOP - St. Vincent Hospital Cancer Center, Green Bay
mi
from
Green Bay, WI
Gabapentin in Treating Peripheral Neuropathy in Cancer Patients Undergoing Chemotherapy
The Efficacy Of Gabapentin In The Management Of Chemotherapy-Induced Peripheral Neuropathy: A Phase III Randomized, Double-Blind, Placebo-Controlled, Crossover Trial
Status: Enrolling
Updated: 7/30/2015
CCOP - St. Vincent Hospital Cancer Center, Green Bay
mi
from
Green Bay, WI
Click here to add this to my saved trials
Gabapentin in Treating Peripheral Neuropathy in Cancer Patients Undergoing Chemotherapy
The Efficacy Of Gabapentin In The Management Of Chemotherapy-Induced Peripheral Neuropathy: A Phase III Randomized, Double-Blind, Placebo-Controlled, Crossover Trial
Status: Enrolling
Updated:  7/30/2015
Allan Blair Cancer Centre
mi
from
Regina,
Gabapentin in Treating Peripheral Neuropathy in Cancer Patients Undergoing Chemotherapy
The Efficacy Of Gabapentin In The Management Of Chemotherapy-Induced Peripheral Neuropathy: A Phase III Randomized, Double-Blind, Placebo-Controlled, Crossover Trial
Status: Enrolling
Updated: 7/30/2015
Allan Blair Cancer Centre
mi
from
Regina,
Click here to add this to my saved trials
Double Blind Trial of Duloxetine in Chronic Fatigue Syndrome
A Randomized, Placebo-Controlled, Double-Blind Trial of Duloxetine in the Treatment of Patients With Chronic Fatigue Syndrome
Status: Enrolling
Updated:  7/31/2015
Women's Health Research Program
mi
from
Cincinnati, OH
Double Blind Trial of Duloxetine in Chronic Fatigue Syndrome
A Randomized, Placebo-Controlled, Double-Blind Trial of Duloxetine in the Treatment of Patients With Chronic Fatigue Syndrome
Status: Enrolling
Updated: 7/31/2015
Women's Health Research Program
mi
from
Cincinnati, OH
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Merz Investigational Site #001184
mi
from
Downey, CA
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Merz Investigational Site #001184
mi
from
Downey, CA
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Merz Investigational Site #001208
mi
from
Long Beach, CA
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Merz Investigational Site #001208
mi
from
Long Beach, CA
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Merz Investigational Site #001244
mi
from
Fairfield, CT
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Merz Investigational Site #001244
mi
from
Fairfield, CT
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Clinical Research Facility
mi
from
Doral, FL
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Clinical Research Facility
mi
from
Doral, FL
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Merz Investigational Site # 001110
mi
from
Overland Park, KA
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Merz Investigational Site # 001110
mi
from
Overland Park, KA
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Merz Investigational Site #001209
mi
from
Columbia, MO
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Merz Investigational Site #001209
mi
from
Columbia, MO
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Merz Investigative Site #001210
mi
from
St. Louis, MO
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Merz Investigative Site #001210
mi
from
St. Louis, MO
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Merz Investigational Site #001198
mi
from
Stratford, NJ
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Merz Investigational Site #001198
mi
from
Stratford, NJ
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Merz Investigational Site #001207
mi
from
Plainview, NY
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Merz Investigational Site #001207
mi
from
Plainview, NY
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Merz Investigational Site #001009
mi
from
Winston-Salem, NC
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Merz Investigational Site #001009
mi
from
Winston-Salem, NC
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Merz Investigative Site #001206
mi
from
Nashville, TN
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Merz Investigative Site #001206
mi
from
Nashville, TN
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Merz Investigational Site #001226
mi
from
Houston, TX
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Merz Investigational Site #001226
mi
from
Houston, TX
Click here to add this to my saved trials
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated:  7/31/2015
Merz Investigational Site #001204
mi
from
Halifax,
Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Leg After a Stroke
Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Lower Limb
Status: Enrolling
Updated: 7/31/2015
Merz Investigational Site #001204
mi
from
Halifax,
Click here to add this to my saved trials
PREMIUM Registry: PRognostic HEModynamIc Profiling in the AcUtely Ill EMergency Department Patient
PROGNOSTIC HEMODYNAMIC PROFILING IN THE ACUTELY ILL EMERGENCY DEPARTMENT PATIENT
Status: Enrolling
Updated:  8/3/2015
Detroit Receiving Hospital/Wayne State University
mi
from
Detroit, MI
PREMIUM Registry: PRognostic HEModynamIc Profiling in the AcUtely Ill EMergency Department Patient
PROGNOSTIC HEMODYNAMIC PROFILING IN THE ACUTELY ILL EMERGENCY DEPARTMENT PATIENT
Status: Enrolling
Updated: 8/3/2015
Detroit Receiving Hospital/Wayne State University
mi
from
Detroit, MI
Click here to add this to my saved trials
PREMIUM Registry: PRognostic HEModynamIc Profiling in the AcUtely Ill EMergency Department Patient
PROGNOSTIC HEMODYNAMIC PROFILING IN THE ACUTELY ILL EMERGENCY DEPARTMENT PATIENT
Status: Enrolling
Updated:  8/3/2015
Henry Ford Hospital
mi
from
Detroit, MI
PREMIUM Registry: PRognostic HEModynamIc Profiling in the AcUtely Ill EMergency Department Patient
PROGNOSTIC HEMODYNAMIC PROFILING IN THE ACUTELY ILL EMERGENCY DEPARTMENT PATIENT
Status: Enrolling
Updated: 8/3/2015
Henry Ford Hospital
mi
from
Detroit, MI
Click here to add this to my saved trials
PREMIUM Registry: PRognostic HEModynamIc Profiling in the AcUtely Ill EMergency Department Patient
PROGNOSTIC HEMODYNAMIC PROFILING IN THE ACUTELY ILL EMERGENCY DEPARTMENT PATIENT
Status: Enrolling
Updated:  8/3/2015
University LaSapienza Rome Sant'Andrea Hospital
mi
from
Rome,
PREMIUM Registry: PRognostic HEModynamIc Profiling in the AcUtely Ill EMergency Department Patient
PROGNOSTIC HEMODYNAMIC PROFILING IN THE ACUTELY ILL EMERGENCY DEPARTMENT PATIENT
Status: Enrolling
Updated: 8/3/2015
University LaSapienza Rome Sant'Andrea Hospital
mi
from
Rome,
Click here to add this to my saved trials
Medication Integration in Treatment of Comorbid Adolescent Substance Users/Attention Deficit Hyperactivity Disorder
Family-Based Protocol for Medication Integration in Treatment of Comorbid ASU/ADHD
Status: Enrolling
Updated:  8/3/2015
Roberto Clemente Center
mi
from
New York, NY
Medication Integration in Treatment of Comorbid Adolescent Substance Users/Attention Deficit Hyperactivity Disorder
Family-Based Protocol for Medication Integration in Treatment of Comorbid ASU/ADHD
Status: Enrolling
Updated: 8/3/2015
Roberto Clemente Center
mi
from
New York, NY
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Family-Based Protocol for Medication Integration in Treatment of Comorbid ASU/ADHD in Routine Care
Family-Based Protocol for Medication Integration in Treatment of Comorbid ASU/ADHD in Routine Care
Status: Enrolling
Updated:  8/3/2015
Roberto Clemente Center
mi
from
New York, NY
Family-Based Protocol for Medication Integration in Treatment of Comorbid ASU/ADHD in Routine Care
Family-Based Protocol for Medication Integration in Treatment of Comorbid ASU/ADHD in Routine Care
Status: Enrolling
Updated: 8/3/2015
Roberto Clemente Center
mi
from
New York, NY
Click here to add this to my saved trials
The Effect of a Large-volume Paracentesis on Fatigue, Sleep, and Quality of Life in Cirrhosis
The Effect of a Large-volume Paracentesis on Fatigue, Sleep, and Quality of Life in Cirrhosis
Status: Enrolling
Updated:  8/3/2015
New York University School of Medicine
mi
from
New York, NY
The Effect of a Large-volume Paracentesis on Fatigue, Sleep, and Quality of Life in Cirrhosis
The Effect of a Large-volume Paracentesis on Fatigue, Sleep, and Quality of Life in Cirrhosis
Status: Enrolling
Updated: 8/3/2015
New York University School of Medicine
mi
from
New York, NY
Click here to add this to my saved trials
Effectiveness of Ankle Foot Orthoses on Gait in Multiple Sclerosis
The Impact of Ankle Foot Orthosis (AFO) on Gait Recovery in Select Individuals With Multiple Sclerosis (MS)
Status: Enrolling
Updated:  8/3/2015
University of Texas Southwestern Medical Center, School of Health Professions
mi
from
Dallas, TX
Effectiveness of Ankle Foot Orthoses on Gait in Multiple Sclerosis
The Impact of Ankle Foot Orthosis (AFO) on Gait Recovery in Select Individuals With Multiple Sclerosis (MS)
Status: Enrolling
Updated: 8/3/2015
University of Texas Southwestern Medical Center, School of Health Professions
mi
from
Dallas, TX
Click here to add this to my saved trials
Safety and Efficacy Study of a Single Dose of NA-1 in Patients Undergoing Endovascular Repair of Ruptured Aneurysms
Phase 2, Multicenter Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study Evaluating a Single Dose of Intravenous NA-1 in Patients With Subarachnoid Hemorrhage Undergoing Endovascular Repair of Ruptured Intracranial Aneurysms
Status: Enrolling
Updated:  8/3/2015
Barrow Neurological Institute
mi
from
Phoenix, AZ
Safety and Efficacy Study of a Single Dose of NA-1 in Patients Undergoing Endovascular Repair of Ruptured Aneurysms
Phase 2, Multicenter Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study Evaluating a Single Dose of Intravenous NA-1 in Patients With Subarachnoid Hemorrhage Undergoing Endovascular Repair of Ruptured Intracranial Aneurysms
Status: Enrolling
Updated: 8/3/2015
Barrow Neurological Institute
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Safety and Efficacy Study of a Single Dose of NA-1 in Patients Undergoing Endovascular Repair of Ruptured Aneurysms
Phase 2, Multicenter Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study Evaluating a Single Dose of Intravenous NA-1 in Patients With Subarachnoid Hemorrhage Undergoing Endovascular Repair of Ruptured Intracranial Aneurysms
Status: Enrolling
Updated:  8/3/2015
Colorado Neurological Institute
mi
from
Englewood, CO
Safety and Efficacy Study of a Single Dose of NA-1 in Patients Undergoing Endovascular Repair of Ruptured Aneurysms
Phase 2, Multicenter Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study Evaluating a Single Dose of Intravenous NA-1 in Patients With Subarachnoid Hemorrhage Undergoing Endovascular Repair of Ruptured Intracranial Aneurysms
Status: Enrolling
Updated: 8/3/2015
Colorado Neurological Institute
mi
from
Englewood, CO
Click here to add this to my saved trials
Safety and Efficacy Study of a Single Dose of NA-1 in Patients Undergoing Endovascular Repair of Ruptured Aneurysms
Phase 2, Multicenter Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study Evaluating a Single Dose of Intravenous NA-1 in Patients With Subarachnoid Hemorrhage Undergoing Endovascular Repair of Ruptured Intracranial Aneurysms
Status: Enrolling
Updated:  8/3/2015
University of Michigan - Neurosurgery
mi
from
Ann Arbor, MI
Safety and Efficacy Study of a Single Dose of NA-1 in Patients Undergoing Endovascular Repair of Ruptured Aneurysms
Phase 2, Multicenter Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study Evaluating a Single Dose of Intravenous NA-1 in Patients With Subarachnoid Hemorrhage Undergoing Endovascular Repair of Ruptured Intracranial Aneurysms
Status: Enrolling
Updated: 8/3/2015
University of Michigan - Neurosurgery
mi
from
Ann Arbor, MI
Click here to add this to my saved trials
Safety and Efficacy Study of a Single Dose of NA-1 in Patients Undergoing Endovascular Repair of Ruptured Aneurysms
Phase 2, Multicenter Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study Evaluating a Single Dose of Intravenous NA-1 in Patients With Subarachnoid Hemorrhage Undergoing Endovascular Repair of Ruptured Intracranial Aneurysms
Status: Enrolling
Updated:  8/3/2015
Oregon Health and Science University
mi
from
Portland, OR
Safety and Efficacy Study of a Single Dose of NA-1 in Patients Undergoing Endovascular Repair of Ruptured Aneurysms
Phase 2, Multicenter Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study Evaluating a Single Dose of Intravenous NA-1 in Patients With Subarachnoid Hemorrhage Undergoing Endovascular Repair of Ruptured Intracranial Aneurysms
Status: Enrolling
Updated: 8/3/2015
Oregon Health and Science University
mi
from
Portland, OR
Click here to add this to my saved trials
Safety and Efficacy Study of a Single Dose of NA-1 in Patients Undergoing Endovascular Repair of Ruptured Aneurysms
Phase 2, Multicenter Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study Evaluating a Single Dose of Intravenous NA-1 in Patients With Subarachnoid Hemorrhage Undergoing Endovascular Repair of Ruptured Intracranial Aneurysms
Status: Enrolling
Updated:  8/3/2015
University of Wisconsin
mi
from
Madison, WI
Safety and Efficacy Study of a Single Dose of NA-1 in Patients Undergoing Endovascular Repair of Ruptured Aneurysms
Phase 2, Multicenter Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study Evaluating a Single Dose of Intravenous NA-1 in Patients With Subarachnoid Hemorrhage Undergoing Endovascular Repair of Ruptured Intracranial Aneurysms
Status: Enrolling
Updated: 8/3/2015
University of Wisconsin
mi
from
Madison, WI
Click here to add this to my saved trials
Safety and Efficacy Study of a Single Dose of NA-1 in Patients Undergoing Endovascular Repair of Ruptured Aneurysms
Phase 2, Multicenter Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study Evaluating a Single Dose of Intravenous NA-1 in Patients With Subarachnoid Hemorrhage Undergoing Endovascular Repair of Ruptured Intracranial Aneurysms
Status: Enrolling
Updated:  8/3/2015
Foothills Medical Centre
mi
from
Calgary,
Safety and Efficacy Study of a Single Dose of NA-1 in Patients Undergoing Endovascular Repair of Ruptured Aneurysms
Phase 2, Multicenter Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Study Evaluating a Single Dose of Intravenous NA-1 in Patients With Subarachnoid Hemorrhage Undergoing Endovascular Repair of Ruptured Intracranial Aneurysms
Status: Enrolling
Updated: 8/3/2015
Foothills Medical Centre
mi
from
Calgary,
Click here to add this to my saved trials
Training Cognitive Control Processes in Older Adults
Pilot Study Using a Video Game to Train Cognitive Control Processes in Healthy Older Adults
Status: Enrolling
Updated:  8/3/2015
Columbia University Medical Center
mi
from
New York, NY
Training Cognitive Control Processes in Older Adults
Pilot Study Using a Video Game to Train Cognitive Control Processes in Healthy Older Adults
Status: Enrolling
Updated: 8/3/2015
Columbia University Medical Center
mi
from
New York, NY
Click here to add this to my saved trials
Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP)
Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP): A Multicenter, Randomized, Placebo-controlled, Double Blind Study
Status: Enrolling
Updated:  8/4/2015
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP)
Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP): A Multicenter, Randomized, Placebo-controlled, Double Blind Study
Status: Enrolling
Updated: 8/4/2015
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
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Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP)
Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP): A Multicenter, Randomized, Placebo-controlled, Double Blind Study
Status: Enrolling
Updated:  8/4/2015
Lahey Clinic
mi
from
Burlington, MA
Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP)
Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP): A Multicenter, Randomized, Placebo-controlled, Double Blind Study
Status: Enrolling
Updated: 8/4/2015
Lahey Clinic
mi
from
Burlington, MA
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Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP)
Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP): A Multicenter, Randomized, Placebo-controlled, Double Blind Study
Status: Enrolling
Updated:  8/4/2015
University of Alabama
mi
from
Birmingham, AL
Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP)
Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP): A Multicenter, Randomized, Placebo-controlled, Double Blind Study
Status: Enrolling
Updated: 8/4/2015
University of Alabama
mi
from
Birmingham, AL
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Mission Connect Mild Traumatic Brain Injury (TBI) Integrated Clinical Protocol
The Mission Connect Mild TBI Translational Research Consortium's Integrated Clinical Protocol
Status: Enrolling
Updated:  8/4/2015
Baylor College of Medicine, Ben Taub General Hospital
mi
from
Houston, TX
Mission Connect Mild Traumatic Brain Injury (TBI) Integrated Clinical Protocol
The Mission Connect Mild TBI Translational Research Consortium's Integrated Clinical Protocol
Status: Enrolling
Updated: 8/4/2015
Baylor College of Medicine, Ben Taub General Hospital
mi
from
Houston, TX
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Mission Connect Mild Traumatic Brain Injury (TBI) Integrated Clinical Protocol
The Mission Connect Mild TBI Translational Research Consortium's Integrated Clinical Protocol
Status: Enrolling
Updated:  8/4/2015
University of Texas Health Science Center at Houston/Memorial Hermann Hospital
mi
from
Houston, TX
Mission Connect Mild Traumatic Brain Injury (TBI) Integrated Clinical Protocol
The Mission Connect Mild TBI Translational Research Consortium's Integrated Clinical Protocol
Status: Enrolling
Updated: 8/4/2015
University of Texas Health Science Center at Houston/Memorial Hermann Hospital
mi
from
Houston, TX
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Safety and Feasibility Study of Targeted Temperature Management After ICH
Safety and Feasibility of a Protocol of Targeted Temperature Management After Intracerebral Hemorrhage
Status: Enrolling
Updated:  8/4/2015
Thomas Jefferson University Hospital
mi
from
Philadelphia, PA
Safety and Feasibility Study of Targeted Temperature Management After ICH
Safety and Feasibility of a Protocol of Targeted Temperature Management After Intracerebral Hemorrhage
Status: Enrolling
Updated: 8/4/2015
Thomas Jefferson University Hospital
mi
from
Philadelphia, PA
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Effect of CPAP on Postoperative Delirium
The Effect of Peri-operative Continuous Positive Airway Pressure (CPAP) on Postoperative Delirium in a Population at High-risk for Obstructive Sleep Apnea (OSA)
Status: Enrolling
Updated:  8/4/2015
Duke University
mi
from
Durham, NC
Effect of CPAP on Postoperative Delirium
The Effect of Peri-operative Continuous Positive Airway Pressure (CPAP) on Postoperative Delirium in a Population at High-risk for Obstructive Sleep Apnea (OSA)
Status: Enrolling
Updated: 8/4/2015
Duke University
mi
from
Durham, NC
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Dosing of Levetiracetam (Keppra) in Neonates
Pharmacokinetics and Safety of 50 mg/kg IV Levetiracetam (Keppra) in Full Term and Preterm Neonates
Status: Enrolling
Updated:  8/5/2015
Cincinnati Children's Hospital Medical Center
mi
from
Cincinnati, OH
Dosing of Levetiracetam (Keppra) in Neonates
Pharmacokinetics and Safety of 50 mg/kg IV Levetiracetam (Keppra) in Full Term and Preterm Neonates
Status: Enrolling
Updated: 8/5/2015
Cincinnati Children's Hospital Medical Center
mi
from
Cincinnati, OH
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Improving Nutrient Intake and Growth in Children With Multiple Food Allergies
Improving Nutrient Intake and Growth in Children With Multiple Food Allergies
Status: Enrolling
Updated:  8/5/2015
Children's Hospital of Wisconsin
mi
from
Milwaukee, WI
Improving Nutrient Intake and Growth in Children With Multiple Food Allergies
Improving Nutrient Intake and Growth in Children With Multiple Food Allergies
Status: Enrolling
Updated: 8/5/2015
Children's Hospital of Wisconsin
mi
from
Milwaukee, WI
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Optical Coherence Tomography Imaging of Post Coil Aneurysm Healing.
Optical Coherence Tomography Imaging of Post Coil Aneurysm Healing.
Status: Enrolling
Updated:  8/5/2015
Beckman Laser Institute University of California Irvine
mi
from
Irvine, CA
Optical Coherence Tomography Imaging of Post Coil Aneurysm Healing.
Optical Coherence Tomography Imaging of Post Coil Aneurysm Healing.
Status: Enrolling
Updated: 8/5/2015
Beckman Laser Institute University of California Irvine
mi
from
Irvine, CA
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Optical Coherence Tomography Imaging of Post Coil Aneurysm Healing.
Optical Coherence Tomography Imaging of Post Coil Aneurysm Healing.
Status: Enrolling
Updated:  8/5/2015
Neurosurgery department, University of California,Irvine
mi
from
Irvine, CA
Optical Coherence Tomography Imaging of Post Coil Aneurysm Healing.
Optical Coherence Tomography Imaging of Post Coil Aneurysm Healing.
Status: Enrolling
Updated: 8/5/2015
Neurosurgery department, University of California,Irvine
mi
from
Irvine, CA
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Complete Occlusion of Coilable Aneurysms
Complete Occlusion of Coilable Aneurysms
Status: Enrolling
Updated:  8/5/2015
Barrow Neurological Institute
mi
from
Phoenix, AZ
Complete Occlusion of Coilable Aneurysms
Complete Occlusion of Coilable Aneurysms
Status: Enrolling
Updated: 8/5/2015
Barrow Neurological Institute
mi
from
Phoenix, AZ
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Complete Occlusion of Coilable Aneurysms
Complete Occlusion of Coilable Aneurysms
Status: Enrolling
Updated:  8/5/2015
SUNY Stony Brook
mi
from
Stony Brook, NY
Complete Occlusion of Coilable Aneurysms
Complete Occlusion of Coilable Aneurysms
Status: Enrolling
Updated: 8/5/2015
SUNY Stony Brook
mi
from
Stony Brook, NY
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Assessing Cerebrovascular Reactivity Based on Cerebral Oximetry: a Pilot Study
Assessing Cerebrovascular Reactivity Based on Cerebral Oximetry
Status: Enrolling
Updated:  8/5/2015
UCI Beckman Laser Institute
mi
from
Irvine, CA
Assessing Cerebrovascular Reactivity Based on Cerebral Oximetry: a Pilot Study
Assessing Cerebrovascular Reactivity Based on Cerebral Oximetry
Status: Enrolling
Updated: 8/5/2015
UCI Beckman Laser Institute
mi
from
Irvine, CA
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Efficacy Study of NH001 in Vegetative State & Minimally Conscious State Following a Traumatic Brain Injury
A Double-blind, Placebo-controlled, Randomized Study of the Safety and Efficacy of NH001 in Improving the Functional Outcome of Patients in a Vegetative State or Minimally Conscious State Following a Severe Traumatic Brain Injury
Status: Enrolling
Updated:  8/6/2015
Spaulding Rehabilitation Hospital
mi
from
Boston, MA
Efficacy Study of NH001 in Vegetative State & Minimally Conscious State Following a Traumatic Brain Injury
A Double-blind, Placebo-controlled, Randomized Study of the Safety and Efficacy of NH001 in Improving the Functional Outcome of Patients in a Vegetative State or Minimally Conscious State Following a Severe Traumatic Brain Injury
Status: Enrolling
Updated: 8/6/2015
Spaulding Rehabilitation Hospital
mi
from
Boston, MA
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Placebo vs. Linoleic Acid Controlled Assessment of Treatment Efficacy in MS
Phase II Study of Linoleic Acid in Relapsing Multiple Sclerosis
Status: Enrolling
Updated:  8/7/2015
University of Rochester
mi
from
Rochester, NY
Placebo vs. Linoleic Acid Controlled Assessment of Treatment Efficacy in MS
Phase II Study of Linoleic Acid in Relapsing Multiple Sclerosis
Status: Enrolling
Updated: 8/7/2015
University of Rochester
mi
from
Rochester, NY
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Treatment Strategy to Prevent Mood Disorders Following Traumatic Brain Injury
Treatment Strategy to Prevent Mood Disorders Following Traumatic Brain Injury
Status: Enrolling
Updated:  8/10/2015
Baylor College of Medicine
mi
from
Houston, TX
Treatment Strategy to Prevent Mood Disorders Following Traumatic Brain Injury
Treatment Strategy to Prevent Mood Disorders Following Traumatic Brain Injury
Status: Enrolling
Updated: 8/10/2015
Baylor College of Medicine
mi
from
Houston, TX
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