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
6,982
archived clinical trials in
Endocrine

LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Carolinas HealthCare System
957
mi
from
Charlotte, NC
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Carolinas HealthCare System
957
mi
from
Charlotte, NC
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Wake Forest University Health Sciences
979
mi
from
Winston-Salem, NC
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Wake Forest University Health Sciences
979
mi
from
Winston-Salem, NC
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Institute for Reproductive Health
730
mi
from
Cincinnati, OH
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Institute for Reproductive Health
730
mi
from
Cincinnati, OH
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
University of Cincinnati Physicians, Inc
725
mi
from
Cincinnati, OH
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
University of Cincinnati Physicians, Inc
725
mi
from
Cincinnati, OH
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
UH Case Medical Center, MacDonald Clinical Trials
894
mi
from
Cleveland, OH
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
UH Case Medical Center, MacDonald Clinical Trials
894
mi
from
Cleveland, OH
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Ohio Reproductive Medicine
810
mi
from
Columbus, OH
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Ohio Reproductive Medicine
810
mi
from
Columbus, OH
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
University of Oklahoma Health Sciences Center, Abington IVF & Genetics, L.P.
158
mi
from
Oklahoma City, OK
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
University of Oklahoma Health Sciences Center, Abington IVF & Genetics, L.P.
158
mi
from
Oklahoma City, OK
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Abington Reproductive Medicine, PC
1227
mi
from
Abington, PA
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Abington Reproductive Medicine, PC
1227
mi
from
Abington, PA
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Main Line Fertility Center
1217
mi
from
Bryn Mawr, PA
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Main Line Fertility Center
1217
mi
from
Bryn Mawr, PA
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Penn State MS Hershey Medical Center, Penn State College of Medicine
1147
mi
from
Hershey, PA
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Penn State MS Hershey Medical Center, Penn State College of Medicine
1147
mi
from
Hershey, PA
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
University of Pittsburgh-Magee Womens Hospital
974
mi
from
Pittsburgh, PA
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
University of Pittsburgh-Magee Womens Hospital
974
mi
from
Pittsburgh, PA
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Fertility Associates of Memphis
478
mi
from
Memphis, TN
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Fertility Associates of Memphis
478
mi
from
Memphis, TN
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Center for Assisted Reproduction
342
mi
from
Bedford, TX
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Center for Assisted Reproduction
342
mi
from
Bedford, TX
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Houston Fertility Institute
569
mi
from
Houston, TX
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Houston Fertility Institute
569
mi
from
Houston, TX
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Center of Reproductive Medicine
588
mi
from
Webster, TX
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Center of Reproductive Medicine
588
mi
from
Webster, TX
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Utah Fertility Center
767
mi
from
Pleasant Grove, UT
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Utah Fertility Center
767
mi
from
Pleasant Grove, UT
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Jones Institute of Reproductive Medicine
1181
mi
from
Norfolk, VA
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Jones Institute of Reproductive Medicine
1181
mi
from
Norfolk, VA
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Olive Fertility Centre
1486
mi
from
Vancouver,
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Olive Fertility Centre
1486
mi
from
Vancouver,
Click here to add this to my saved trials
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Lyndhurst Clinical Research
971
mi
from
Winston-Salem, NC
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Lyndhurst Clinical Research
971
mi
from
Winston-Salem, NC
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LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated:  12/31/1969
Columbia Fertility Associates
1126
mi
from
Washington,
LutrePulse Hypogonadotropic Hypogonadism
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating Three Doses of Subcutaneous Pulsatile GnRH Administered Via OmniPod Pump for Ovulation Induction in Female Subjects With Primary Amenorrhea With Hypogonadotropic Hypogonadism
Status: Enrolling
Updated: 12/31/1969
Columbia Fertility Associates
1126
mi
from
Washington,
Click here to add this to my saved trials
Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated:  12/31/1969
Barbara Davis Center for Diabetes
402
mi
from
Aurora, CO
Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated: 12/31/1969
Barbara Davis Center for Diabetes
402
mi
from
Aurora, CO
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Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated:  12/31/1969
Oregon Health and Science University
1383
mi
from
Portland, OR
Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated: 12/31/1969
Oregon Health and Science University
1383
mi
from
Portland, OR
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Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated:  12/31/1969
Riley Hospital for Children at Indiana University Health
642
mi
from
Indianapolis, IN
Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated: 12/31/1969
Riley Hospital for Children at Indiana University Health
642
mi
from
Indianapolis, IN
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Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated:  12/31/1969
University of Florida
1049
mi
from
Gainesville, FL
Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated: 12/31/1969
University of Florida
1049
mi
from
Gainesville, FL
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Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated:  12/31/1969
Univ of Minnesota
552
mi
from
Minneapolis, MN
Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated: 12/31/1969
Univ of Minnesota
552
mi
from
Minneapolis, MN
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Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated:  12/31/1969
Univ of Pennsylvania
1223
mi
from
Philadelphia, PA
Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated: 12/31/1969
Univ of Pennsylvania
1223
mi
from
Philadelphia, PA
Click here to add this to my saved trials
Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated:  12/31/1969
UPA Buffalo
1056
mi
from
Buffalo, NY
Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated: 12/31/1969
UPA Buffalo
1056
mi
from
Buffalo, NY
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Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated:  12/31/1969
Yale University
1344
mi
from
New Haven, CT
Efficacy and Safety of Nasal Glucagon for Treatment of Hypoglycemia in Adults
Efficacy and Safety of Nasal Glucagon for Treatment of Insulin Induced Hypoglycemia in Adults With Diabetes
Status: Enrolling
Updated: 12/31/1969
Yale University
1344
mi
from
New Haven, CT
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EC17 for Intraoperative Imaging for Parathyroidectomy
A Pilot & Feasibility Study of the Imaging Potential of EC17 in Subjects Undergoing Parathyroidectomy for Primary Hyperparathyroidism.
Status: Enrolling
Updated:  12/31/1969
Hospital of the University of Pennsylvania
1223
mi
from
Philadelphia, PA
EC17 for Intraoperative Imaging for Parathyroidectomy
A Pilot & Feasibility Study of the Imaging Potential of EC17 in Subjects Undergoing Parathyroidectomy for Primary Hyperparathyroidism.
Status: Enrolling
Updated: 12/31/1969
Hospital of the University of Pennsylvania
1223
mi
from
Philadelphia, PA
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Effects of Interrupting Sedentary Time on Glycemic Control in Older Overweight and Obese Adults
Effects of Interrupting Sedentary Time on Glycemic Control in Older Overweight and Obese Adults
Status: Enrolling
Updated:  12/31/1969
University of Colorado Denver Anschutz Medical Campus
402
mi
from
Aurora, CO
Effects of Interrupting Sedentary Time on Glycemic Control in Older Overweight and Obese Adults
Effects of Interrupting Sedentary Time on Glycemic Control in Older Overweight and Obese Adults
Status: Enrolling
Updated: 12/31/1969
University of Colorado Denver Anschutz Medical Campus
402
mi
from
Aurora, CO
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Study of Adrenalectomy Versus Observation for Subclinical Hypercortisolism
Randomized Control Trial of Adrenalectomy Versus Observation for Subclinical Hypercortisolism
Status: Enrolling
Updated:  12/31/1969
National Institutes of Health Clinical Center, 9000 Rockville Pike
1123
mi
from
Bethesda, MD
Study of Adrenalectomy Versus Observation for Subclinical Hypercortisolism
Randomized Control Trial of Adrenalectomy Versus Observation for Subclinical Hypercortisolism
Status: Enrolling
Updated: 12/31/1969
National Institutes of Health Clinical Center, 9000 Rockville Pike
1123
mi
from
Bethesda, MD
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Markers of Pubertal Suppression During Therapy for Precocious Puberty
Markers of Adequate Pubertal Suppression During Supprelin LA Therapy for Central Precocious Puberty
Status: Enrolling
Updated:  12/31/1969
Univ of Minnesota
552
mi
from
Minneapolis, MN
Markers of Pubertal Suppression During Therapy for Precocious Puberty
Markers of Adequate Pubertal Suppression During Supprelin LA Therapy for Central Precocious Puberty
Status: Enrolling
Updated: 12/31/1969
Univ of Minnesota
552
mi
from
Minneapolis, MN
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Markers of Pubertal Suppression During Therapy for Precocious Puberty
Markers of Adequate Pubertal Suppression During Supprelin LA Therapy for Central Precocious Puberty
Status: Enrolling
Updated:  12/31/1969
Atlantic Center for Research
1262
mi
from
Morristown, NJ
Markers of Pubertal Suppression During Therapy for Precocious Puberty
Markers of Adequate Pubertal Suppression During Supprelin LA Therapy for Central Precocious Puberty
Status: Enrolling
Updated: 12/31/1969
Atlantic Center for Research
1262
mi
from
Morristown, NJ
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Phase 2 Clinical Trial of SGS-742 Therapy in Succinic Semialdehyde Dehydrogenase Deficiency
Phase 2 Clinical Trial of SGS-742 Therapy in Succinic Semialdehyde Dehydrogenase Deficiency
Status: Enrolling
Updated:  12/31/1969
National Institutes of Health Clinical Center, 9000 Rockville Pike
1123
mi
from
Bethesda, MD
Phase 2 Clinical Trial of SGS-742 Therapy in Succinic Semialdehyde Dehydrogenase Deficiency
Phase 2 Clinical Trial of SGS-742 Therapy in Succinic Semialdehyde Dehydrogenase Deficiency
Status: Enrolling
Updated: 12/31/1969
National Institutes of Health Clinical Center, 9000 Rockville Pike
1123
mi
from
Bethesda, MD
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Phase 2 Clinical Trial of SGS-742 Therapy in Succinic Semialdehyde Dehydrogenase Deficiency
Phase 2 Clinical Trial of SGS-742 Therapy in Succinic Semialdehyde Dehydrogenase Deficiency
Status: Enrolling
Updated:  12/31/1969
Washington State University
1186
mi
from
Pullman, WA
Phase 2 Clinical Trial of SGS-742 Therapy in Succinic Semialdehyde Dehydrogenase Deficiency
Phase 2 Clinical Trial of SGS-742 Therapy in Succinic Semialdehyde Dehydrogenase Deficiency
Status: Enrolling
Updated: 12/31/1969
Washington State University
1186
mi
from
Pullman, WA
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Observational Study of Insulin Resistance and Muscle Wasting After Burn Injury
Project 4: Molecular Mechanisms in Burn-induced Insulin Resistance in Humans
Status: Enrolling
Updated:  12/31/1969
Massachusetts General Hospital
1443
mi
from
Boston, MA
Observational Study of Insulin Resistance and Muscle Wasting After Burn Injury
Project 4: Molecular Mechanisms in Burn-induced Insulin Resistance in Humans
Status: Enrolling
Updated: 12/31/1969
Massachusetts General Hospital
1443
mi
from
Boston, MA
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Diabetes Prevention Program for Obese Latino Youth
Community-Based Diabetes Prevention Program for Obese Latino Youth: Every Little Step Counts
Status: Enrolling
Updated:  12/31/1969
Arizona State University
852
mi
from
Phoenix, AZ
Diabetes Prevention Program for Obese Latino Youth
Community-Based Diabetes Prevention Program for Obese Latino Youth: Every Little Step Counts
Status: Enrolling
Updated: 12/31/1969
Arizona State University
852
mi
from
Phoenix, AZ
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Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
Banner University Medical Center, Phoenix Advanced Lung Disease Institute
852
mi
from
Phoenix, AZ
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
Banner University Medical Center, Phoenix Advanced Lung Disease Institute
852
mi
from
Phoenix, AZ
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Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
Arizona Pulmonary Specialists, Ltd.
851
mi
from
Phoenix, AZ
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
Arizona Pulmonary Specialists, Ltd.
851
mi
from
Phoenix, AZ
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Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
Cedars-Sinai Medical Center
1175
mi
from
Beverly Hills, CA
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
Cedars-Sinai Medical Center
1175
mi
from
Beverly Hills, CA
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Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
VA Healthcare System of Greater Los Angeles
1179
mi
from
Los Angeles, CA
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
VA Healthcare System of Greater Los Angeles
1179
mi
from
Los Angeles, CA
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Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
University of California Davis Medical Center - Division of Pulmonary and Critical Care
1281
mi
from
Sacramento, CA
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
University of California Davis Medical Center - Division of Pulmonary and Critical Care
1281
mi
from
Sacramento, CA
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Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
Harbor UCLA Medical Center
1176
mi
from
Torrance, CA
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
Harbor UCLA Medical Center
1176
mi
from
Torrance, CA
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Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
Cleveland Clinic Florida
1299
mi
from
Weston, FL
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
Cleveland Clinic Florida
1299
mi
from
Weston, FL
Click here to add this to my saved trials
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
Maine Medical Center - Division of Pulmonary and Critical Care Medicine
1490
mi
from
Portland, ME
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
Maine Medical Center - Division of Pulmonary and Critical Care Medicine
1490
mi
from
Portland, ME
Click here to add this to my saved trials
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
Tufts Medical Center
1443
mi
from
Boston, MA
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
Tufts Medical Center
1443
mi
from
Boston, MA
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Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
Brigham and Women's Hosp
1444
mi
from
Boston, MA
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
Brigham and Women's Hosp
1444
mi
from
Boston, MA
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Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
Boston University School of Medicine
1443
mi
from
Boston, MA
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
Boston University School of Medicine
1443
mi
from
Boston, MA
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Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
Winthrop University Hospital
1306
mi
from
Mineola, NY
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
Winthrop University Hospital
1306
mi
from
Mineola, NY
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Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated:  12/31/1969
Weill Cornell Medical Center
1289
mi
from
New York, NY
Bardoxolone Methyl Evaluation in Patients With Pulmonary Hypertension (PH) - LARIAT
A Dose-Ranging Study of the Efficacy and Safety of Bardoxolone Methyl in Patients With Pulmonary Hypertension
Status: Enrolling
Updated: 12/31/1969
Weill Cornell Medical Center
1289
mi
from
New York, NY
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