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
10,154
archived clinical trials in
Other Indications

Efficacy and Safety of a Hospital Walking Program for Older Adults
Efficacy and Safety of a Hospital Walking Program for Older Adults
Status: Enrolling
Updated:  2/23/2016
VA Medical Center, Birmingham
mi
from
Birmingham, AL
Efficacy and Safety of a Hospital Walking Program for Older Adults
Efficacy and Safety of a Hospital Walking Program for Older Adults
Status: Enrolling
Updated: 2/23/2016
VA Medical Center, Birmingham
mi
from
Birmingham, AL
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Effect of a Transcutaneous Electrical Nerve Stimulation (TENS) Device on Overall Facial Appearance
Effect of a Transcutaneous Electrical Nerve Stimulation (TENS) Device on Overall Facial Appearance
Status: Enrolling
Updated:  2/23/2016
Sadick Research Group
mi
from
New York, NJ
Effect of a Transcutaneous Electrical Nerve Stimulation (TENS) Device on Overall Facial Appearance
Effect of a Transcutaneous Electrical Nerve Stimulation (TENS) Device on Overall Facial Appearance
Status: Enrolling
Updated: 2/23/2016
Sadick Research Group
mi
from
New York, NJ
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PASS Study To Evaluate The Potential Of Zithromax To Cause Ocular Problems In Pediatric Patients
Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/Tonsillitis
Status: Enrolling
Updated:  2/23/2016
Martel Eye Medical Group
mi
from
Rancho Cordova, CA
PASS Study To Evaluate The Potential Of Zithromax To Cause Ocular Problems In Pediatric Patients
Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/Tonsillitis
Status: Enrolling
Updated: 2/23/2016
Martel Eye Medical Group
mi
from
Rancho Cordova, CA
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PASS Study To Evaluate The Potential Of Zithromax To Cause Ocular Problems In Pediatric Patients
Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/Tonsillitis
Status: Enrolling
Updated:  2/23/2016
Ann & Robert H. Lurie Children's Hospital of Chicago
mi
from
Chicago, IL
PASS Study To Evaluate The Potential Of Zithromax To Cause Ocular Problems In Pediatric Patients
Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/Tonsillitis
Status: Enrolling
Updated: 2/23/2016
Ann & Robert H. Lurie Children's Hospital of Chicago
mi
from
Chicago, IL
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PASS Study To Evaluate The Potential Of Zithromax To Cause Ocular Problems In Pediatric Patients
Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/Tonsillitis
Status: Enrolling
Updated:  2/23/2016
Infant Welfare Society of Chicago
mi
from
Chicago, IL
PASS Study To Evaluate The Potential Of Zithromax To Cause Ocular Problems In Pediatric Patients
Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/Tonsillitis
Status: Enrolling
Updated: 2/23/2016
Infant Welfare Society of Chicago
mi
from
Chicago, IL
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PASS Study To Evaluate The Potential Of Zithromax To Cause Ocular Problems In Pediatric Patients
Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/Tonsillitis
Status: Enrolling
Updated:  2/23/2016
Outpatient Center in Lincoln Park
mi
from
Chicago, IL
PASS Study To Evaluate The Potential Of Zithromax To Cause Ocular Problems In Pediatric Patients
Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/Tonsillitis
Status: Enrolling
Updated: 2/23/2016
Outpatient Center in Lincoln Park
mi
from
Chicago, IL
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PASS Study To Evaluate The Potential Of Zithromax To Cause Ocular Problems In Pediatric Patients
Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/Tonsillitis
Status: Enrolling
Updated:  2/23/2016
Murray Pediatrics
mi
from
Murray, UT
PASS Study To Evaluate The Potential Of Zithromax To Cause Ocular Problems In Pediatric Patients
Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/Tonsillitis
Status: Enrolling
Updated: 2/23/2016
Murray Pediatrics
mi
from
Murray, UT
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PASS Study To Evaluate The Potential Of Zithromax To Cause Ocular Problems In Pediatric Patients
Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/Tonsillitis
Status: Enrolling
Updated:  2/23/2016
Daynes Eye and Lasik
mi
from
Salt Lake City, UT
PASS Study To Evaluate The Potential Of Zithromax To Cause Ocular Problems In Pediatric Patients
Ocular Effects Of Azithromycin Oral Solution In Pediatric Patients With Pharyngitis/Tonsillitis
Status: Enrolling
Updated: 2/23/2016
Daynes Eye and Lasik
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated:  2/24/2016
Novartis Investigative Site
mi
from
Decatur, GA
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated: 2/24/2016
Novartis Investigative Site
mi
from
Decatur, GA
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Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated:  2/24/2016
Novartis Investigator Site
mi
from
Chicago, IL
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated: 2/24/2016
Novartis Investigator Site
mi
from
Chicago, IL
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Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated:  2/24/2016
Novartis Investigative site
mi
from
Boston, MA
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated: 2/24/2016
Novartis Investigative site
mi
from
Boston, MA
Click here to add this to my saved trials
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated:  2/24/2016
Novartis Investigative Site
mi
from
Omaha, NE
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated: 2/24/2016
Novartis Investigative Site
mi
from
Omaha, NE
Click here to add this to my saved trials
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated:  2/24/2016
Novartis Investigative Site
mi
from
Staten Island, NY
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated: 2/24/2016
Novartis Investigative Site
mi
from
Staten Island, NY
Click here to add this to my saved trials
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated:  2/24/2016
Novartis Investigative Site
mi
from
Nashville, TN
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated: 2/24/2016
Novartis Investigative Site
mi
from
Nashville, TN
Click here to add this to my saved trials
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated:  2/24/2016
Novartis Investigative Site
mi
from
Sacramento, CA
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated: 2/24/2016
Novartis Investigative Site
mi
from
Sacramento, CA
Click here to add this to my saved trials
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated:  2/24/2016
Novartis Investigative Site
mi
from
Westmead,
Long-term, Safety and Tolerability Study of AFQ056 in Adolescent Patients With Fragile X Syndrome (Open-label)
An Open-label Study to Evaluate the Long-term Safety and Tolerability of AFQ056 in Adolescent Patients With Fragile X Syndrome
Status: Enrolling
Updated: 2/24/2016
Novartis Investigative Site
mi
from
Westmead,
Click here to add this to my saved trials
Randomized Trial Comparing Partial Resection of Inferior Turbinate(PRIT) and Radiofrequency Ablation(RFA) for Inferior Turbinate Reduction
A Randomized Trial Comparing Two Surgical Techniques for Inferior Turbinate Reduction
Status: Enrolling
Updated:  2/24/2016
Weill Medical College of Cornell University
mi
from
New York, NY
Randomized Trial Comparing Partial Resection of Inferior Turbinate(PRIT) and Radiofrequency Ablation(RFA) for Inferior Turbinate Reduction
A Randomized Trial Comparing Two Surgical Techniques for Inferior Turbinate Reduction
Status: Enrolling
Updated: 2/24/2016
Weill Medical College of Cornell University
mi
from
New York, NY
Click here to add this to my saved trials
Commercial Lidocaine Patch as a Treatment for Ear-ringing
Transdermal Lidocaine as a Treatment for Tinnitus
Status: Enrolling
Updated:  2/25/2016
UC Davis Department of Otolaryngology
mi
from
Sacramento, CA
Commercial Lidocaine Patch as a Treatment for Ear-ringing
Transdermal Lidocaine as a Treatment for Tinnitus
Status: Enrolling
Updated: 2/25/2016
UC Davis Department of Otolaryngology
mi
from
Sacramento, CA
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Effect of Formoterol on the Counterregulatory Hormonal Response to Hypoglycemia in Type 1 Diabetes.
The Effect of the Beta 2 Agonist, Formoterol, on Recovery From Hypoglycemia
Status: Enrolling
Updated:  2/26/2016
Yale University School of Medicine
mi
from
New Haven, CT
Effect of Formoterol on the Counterregulatory Hormonal Response to Hypoglycemia in Type 1 Diabetes.
The Effect of the Beta 2 Agonist, Formoterol, on Recovery From Hypoglycemia
Status: Enrolling
Updated: 2/26/2016
Yale University School of Medicine
mi
from
New Haven, CT
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Risk Factors and Potential Causes of Eustachian Tube Dysfunction in Adults
Risk Factors and Potential Causes of Eustachian Tube Dysfunction in Adults With Clinically Diagnosed Chronic Otitis Media With Effusion and/or Eustachian Tube Dysfunction
Status: Enrolling
Updated:  2/26/2016
Middle Ear Physiology Laboratory of Children's Hospital of PIttsburgh of UPMC
mi
from
Pittsburgh, PA
Risk Factors and Potential Causes of Eustachian Tube Dysfunction in Adults
Risk Factors and Potential Causes of Eustachian Tube Dysfunction in Adults With Clinically Diagnosed Chronic Otitis Media With Effusion and/or Eustachian Tube Dysfunction
Status: Enrolling
Updated: 2/26/2016
Middle Ear Physiology Laboratory of Children's Hospital of PIttsburgh of UPMC
mi
from
Pittsburgh, PA
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A Study of Patients With Sanfilippo Syndrome Type A (MPS IIIA)
A Longitudinal, Prospective, Natural History Study of Patients With Sanfilippo Syndrome Type A (MPS IIIA)
Status: Enrolling
Updated:  2/29/2016
Univ of Minnesota
mi
from
Minneapolis, MN
A Study of Patients With Sanfilippo Syndrome Type A (MPS IIIA)
A Longitudinal, Prospective, Natural History Study of Patients With Sanfilippo Syndrome Type A (MPS IIIA)
Status: Enrolling
Updated: 2/29/2016
Univ of Minnesota
mi
from
Minneapolis, MN
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Factors Associated With End Stage Liver Disease
Factors Associated With End Stage Liver Disease
Status: Enrolling
Updated:  3/1/2016
NYU School of Medicine, Schwartz Health Care Center Suite 4C
mi
from
New York, NY
Factors Associated With End Stage Liver Disease
Factors Associated With End Stage Liver Disease
Status: Enrolling
Updated: 3/1/2016
NYU School of Medicine, Schwartz Health Care Center Suite 4C
mi
from
New York, NY
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EMA-Defined Tinnitus Subgroups
Identification of Unique Tinnitus Subgroups Using Ecological Momentary Assessment (EMA).
Status: Enrolling
Updated:  3/1/2016
Washington University
mi
from
St. Louis, MO
EMA-Defined Tinnitus Subgroups
Identification of Unique Tinnitus Subgroups Using Ecological Momentary Assessment (EMA).
Status: Enrolling
Updated: 3/1/2016
Washington University
mi
from
St. Louis, MO
Click here to add this to my saved trials
Littlears Auditory Questionnaire: Validation Study in CI Children
Littlears Auditory Questionnaire Validation Study in CI Children With LittlEARS My Diary: Language: North American English
Status: Enrolling
Updated:  3/4/2016
Georgia Health Sciences University
mi
from
Augusta, GA
Littlears Auditory Questionnaire: Validation Study in CI Children
Littlears Auditory Questionnaire Validation Study in CI Children With LittlEARS My Diary: Language: North American English
Status: Enrolling
Updated: 3/4/2016
Georgia Health Sciences University
mi
from
Augusta, GA
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Littlears Auditory Questionnaire: Validation Study in CI Children
Littlears Auditory Questionnaire Validation Study in CI Children With LittlEARS My Diary: Language: North American English
Status: Enrolling
Updated:  3/4/2016
University of North Carolina-Chapel Hill/CCCDP
mi
from
Durham, NC
Littlears Auditory Questionnaire: Validation Study in CI Children
Littlears Auditory Questionnaire Validation Study in CI Children With LittlEARS My Diary: Language: North American English
Status: Enrolling
Updated: 3/4/2016
University of North Carolina-Chapel Hill/CCCDP
mi
from
Durham, NC
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Littlears Auditory Questionnaire: Validation Study in CI Children
Littlears Auditory Questionnaire Validation Study in CI Children With LittlEARS My Diary: Language: North American English
Status: Enrolling
Updated:  3/4/2016
Vanderbilt University
mi
from
Nashville, TN
Littlears Auditory Questionnaire: Validation Study in CI Children
Littlears Auditory Questionnaire Validation Study in CI Children With LittlEARS My Diary: Language: North American English
Status: Enrolling
Updated: 3/4/2016
Vanderbilt University
mi
from
Nashville, TN
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Littlears Auditory Questionnaire: Validation Study in CI Children
Littlears Auditory Questionnaire Validation Study in CI Children With LittlEARS My Diary: Language: North American English
Status: Enrolling
Updated:  3/4/2016
Cook Children's Medical Center
mi
from
Fort Worth, TX
Littlears Auditory Questionnaire: Validation Study in CI Children
Littlears Auditory Questionnaire Validation Study in CI Children With LittlEARS My Diary: Language: North American English
Status: Enrolling
Updated: 3/4/2016
Cook Children's Medical Center
mi
from
Fort Worth, TX
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Littlears Auditory Questionnaire: Validation Study in CI Children
Littlears Auditory Questionnaire Validation Study in CI Children With LittlEARS My Diary: Language: North American English
Status: Enrolling
Updated:  3/4/2016
Medical College of Wisconsin
mi
from
Milwaukee, WI
Littlears Auditory Questionnaire: Validation Study in CI Children
Littlears Auditory Questionnaire Validation Study in CI Children With LittlEARS My Diary: Language: North American English
Status: Enrolling
Updated: 3/4/2016
Medical College of Wisconsin
mi
from
Milwaukee, WI
Click here to add this to my saved trials
Biomarkers of Aging as Predictors of Kidney Transplant Function
Clinical Utility of Biomarkers of Aging as Predictors of Kidney Graft Function in Extended Criteria Organ Recipients
Status: Enrolling
Updated:  3/6/2016
UNC Hospitals
mi
from
Chapel Hill, NC
Biomarkers of Aging as Predictors of Kidney Transplant Function
Clinical Utility of Biomarkers of Aging as Predictors of Kidney Graft Function in Extended Criteria Organ Recipients
Status: Enrolling
Updated: 3/6/2016
UNC Hospitals
mi
from
Chapel Hill, NC
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Biomarkers of Aging as Predictors of Kidney Transplant Function
Clinical Utility of Biomarkers of Aging as Predictors of Kidney Graft Function in Extended Criteria Organ Recipients
Status: Enrolling
Updated:  3/6/2016
Wake Forest Baptist Health, Abdominal Organ Transplant Program
mi
from
Winston-Salem, NC
Biomarkers of Aging as Predictors of Kidney Transplant Function
Clinical Utility of Biomarkers of Aging as Predictors of Kidney Graft Function in Extended Criteria Organ Recipients
Status: Enrolling
Updated: 3/6/2016
Wake Forest Baptist Health, Abdominal Organ Transplant Program
mi
from
Winston-Salem, NC
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Study of Chokeberry to Reduce Cardiovascular Disease Risk in Former Smokers
The Effect of Chokeberry Polyphenols on Biomarkers of Cardiovascular Disease and Antioxidant Defenses in Former Smokers
Status: Enrolling
Updated:  3/8/2016
Roy E. Jones Building
mi
from
Storrs, CT
Study of Chokeberry to Reduce Cardiovascular Disease Risk in Former Smokers
The Effect of Chokeberry Polyphenols on Biomarkers of Cardiovascular Disease and Antioxidant Defenses in Former Smokers
Status: Enrolling
Updated: 3/8/2016
Roy E. Jones Building
mi
from
Storrs, CT
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Treating Cancer-Related Fatigue Through Systematic Light Exposure
Treating Cancer-Related Fatigue Through Systematic Light Exposure
Status: Enrolling
Updated:  3/8/2016
Hackensack University Medical Center
mi
from
Hackensack, NJ
Treating Cancer-Related Fatigue Through Systematic Light Exposure
Treating Cancer-Related Fatigue Through Systematic Light Exposure
Status: Enrolling
Updated: 3/8/2016
Hackensack University Medical Center
mi
from
Hackensack, NJ
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Treating Cancer-Related Fatigue Through Systematic Light Exposure
Treating Cancer-Related Fatigue Through Systematic Light Exposure
Status: Enrolling
Updated:  3/8/2016
Icahn School of Medicine at Mount Sinai
mi
from
New York, NY
Treating Cancer-Related Fatigue Through Systematic Light Exposure
Treating Cancer-Related Fatigue Through Systematic Light Exposure
Status: Enrolling
Updated: 3/8/2016
Icahn School of Medicine at Mount Sinai
mi
from
New York, NY
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Fat Distribution and Glucose Metabolism in Williams Syndrome
Characterization of Fat Distribution and Glucose Metabolism in Individuals With and Without Williams Syndrome
Status: Enrolling
Updated:  3/10/2016
Massachusetts General Hospital
mi
from
Boston, MA
Fat Distribution and Glucose Metabolism in Williams Syndrome
Characterization of Fat Distribution and Glucose Metabolism in Individuals With and Without Williams Syndrome
Status: Enrolling
Updated: 3/10/2016
Massachusetts General Hospital
mi
from
Boston, MA
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Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers
A Multi-center Randomized Controlled Clinical Trial Evaluating Two Application Regimens of Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers.
Status: Enrolling
Updated:  3/14/2016
Eric J. Lullove DPM
mi
from
Boca Raton, FL
Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers
A Multi-center Randomized Controlled Clinical Trial Evaluating Two Application Regimens of Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers.
Status: Enrolling
Updated: 3/14/2016
Eric J. Lullove DPM
mi
from
Boca Raton, FL
Click here to add this to my saved trials
Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers
A Multi-center Randomized Controlled Clinical Trial Evaluating Two Application Regimens of Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers.
Status: Enrolling
Updated:  3/14/2016
MetroWest Medical Center
mi
from
Framingham, MA
Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers
A Multi-center Randomized Controlled Clinical Trial Evaluating Two Application Regimens of Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers.
Status: Enrolling
Updated: 3/14/2016
MetroWest Medical Center
mi
from
Framingham, MA
Click here to add this to my saved trials
Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers
A Multi-center Randomized Controlled Clinical Trial Evaluating Two Application Regimens of Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers.
Status: Enrolling
Updated:  3/14/2016
St. Vincent's Health Center
mi
from
Erie, PA
Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers
A Multi-center Randomized Controlled Clinical Trial Evaluating Two Application Regimens of Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers.
Status: Enrolling
Updated: 3/14/2016
St. Vincent's Health Center
mi
from
Erie, PA
Click here to add this to my saved trials
Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers
A Multi-center Randomized Controlled Clinical Trial Evaluating Two Application Regimens of Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers.
Status: Enrolling
Updated:  3/14/2016
Armstrong County Memorial Hospital
mi
from
Kittanning, PA
Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers
A Multi-center Randomized Controlled Clinical Trial Evaluating Two Application Regimens of Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers.
Status: Enrolling
Updated: 3/14/2016
Armstrong County Memorial Hospital
mi
from
Kittanning, PA
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Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers
A Multi-center Randomized Controlled Clinical Trial Evaluating Two Application Regimens of Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers.
Status: Enrolling
Updated:  3/14/2016
St. Johns Wound Center
mi
from
Tulsa, OK
Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers
A Multi-center Randomized Controlled Clinical Trial Evaluating Two Application Regimens of Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers.
Status: Enrolling
Updated: 3/14/2016
St. Johns Wound Center
mi
from
Tulsa, OK
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Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
University of South Alabama Medical Center
mi
from
Mobile, AL
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
University of South Alabama Medical Center
mi
from
Mobile, AL
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Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
Arrowhead Regional Medical Center
mi
from
Redlands, CA
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
Arrowhead Regional Medical Center
mi
from
Redlands, CA
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Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
Shands Burn Center at University of Florida
mi
from
Gainesville, FL
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
Shands Burn Center at University of Florida
mi
from
Gainesville, FL
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Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
Loyola University Medical Center
mi
from
Maywood, IL
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
Loyola University Medical Center
mi
from
Maywood, IL
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Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
The Plastic Surgery Institute - Southern Illinois Univ. School of Medicine
mi
from
Springfield, IL
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
The Plastic Surgery Institute - Southern Illinois Univ. School of Medicine
mi
from
Springfield, IL
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Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
University of Kansas Medical Center
mi
from
Kansas City, KA
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
University of Kansas Medical Center
mi
from
Kansas City, KA
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Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
Johns Hopkins Burn Center
mi
from
Baltimore, MD
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
Johns Hopkins Burn Center
mi
from
Baltimore, MD
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Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
University of Missouri Healthcare - Dept. of Surgery
mi
from
Columbia, MO
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
University of Missouri Healthcare - Dept. of Surgery
mi
from
Columbia, MO
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Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated:  3/15/2016
Wake Forest University - Department of General Surgery
mi
from
Winston-Salem, NC
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Prospective Evaluation of the Effects of Topical Therapy With Sulfamylon® For 5% Topical Solution on Autograft Healing in Subjects With Thermal Injuries Requiring Meshed Autografts: A Comparison to a Historical Control Group
Status: Enrolling
Updated: 3/15/2016
Wake Forest University - Department of General Surgery
mi
from
Winston-Salem, NC
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hCAP18 Levels and Vitamin D Deficiency in Healthy Subjects
hCAP18 Levels and Vitamin D Deficiency in Healthy Subjects
Status: Enrolling
Updated:  3/15/2016
Massachusetts General Hospital
mi
from
Boston, MA
hCAP18 Levels and Vitamin D Deficiency in Healthy Subjects
hCAP18 Levels and Vitamin D Deficiency in Healthy Subjects
Status: Enrolling
Updated: 3/15/2016
Massachusetts General Hospital
mi
from
Boston, MA
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Combination Chemotherapy in Treating Young Patients With Down Syndrome and Acute Myeloid Leukemia or Myelodysplastic Syndromes
The Treatment of Down Syndrome Children With Acute Myeloid Leukemia (AML) and Myelodysplastic Syndromes (MDS) Under the Age of 4 Years
Status: Enrolling
Updated:  3/16/2016
Phoenix Children's Hospital
mi
from
Phoenix, AZ
Combination Chemotherapy in Treating Young Patients With Down Syndrome and Acute Myeloid Leukemia or Myelodysplastic Syndromes
The Treatment of Down Syndrome Children With Acute Myeloid Leukemia (AML) and Myelodysplastic Syndromes (MDS) Under the Age of 4 Years
Status: Enrolling
Updated: 3/16/2016
Phoenix Children's Hospital
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from
Phoenix, AZ
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