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We've found
184,457
clinical trials

Children Whose Mothers Received 17P and Those Who Received Vehicle in the 17P Efficacy Trial Clinical Trial
A Prospective, Noninterventional Follow-Up Study of Children Aged 23 to 25 Months, Born to Mothers Who Received Hydroxyprogesterone Caproate Injection, 250 mg/mL, or Vehicle for Prevention of Preterm Birth
Status: Enrolling, Phase
Updated: 4/9/2018
Watching Over Mothers and Babies Foundation
mi
from
Tucson, AZ
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Hematology Clinical Trial
Topical Timolol 0.5% Solution for Proliferating Infantile Hemangiomas
Status: Enrolling, Phase
Updated: 6/18/2010
Oregon Health and Science University
mi
from
Portland, OR
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Gastroenterology Clinical Trial
Longitudinal Study of Mitochondrial Hepatopathies
Status: Enrolling, Phase
Updated: 12/31/1969
Mount Sinai Hospital
mi
from
New York, NY
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Gastroenterology Clinical Trial
Longitudinal Study of Mitochondrial Hepatopathies
Status: Enrolling, Phase
Updated: 12/31/1969
Johns Hopkins School of Medicine
mi
from
Baltimore, MD
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Breast Cancer Clinical Trial
RO4929097 And Exemestane in Treating Pre- and Postmenopausal Patients With Advanced or Metastatic Breast Cancer
Status: Enrolling
Updated: 11/10/2011
Winship Cancer Institute of Emory University
mi
from
Egleston, GA
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Reproductive Clinical Trial
A Prospective Natural History Study of Patients With Syringomyelia
Status: Enrolling, Phase
Updated: 12/31/1969
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
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Her2 Negative Breast Cancer Patients Clinical Trial
Trial of Exemestane +/- MM-121 in Postmenopausal Women With Locally Advanced or Metastatic Estrogen Receptor Positive and/or Progesterone Receptor Positive Her2 Negative Breast Cancer
Status: Enrolling
Updated: 3/1/2013
Achieve Clinical Research
mi
from
Birmingham, AL
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Her2 Negative Breast Cancer Patients Clinical Trial
Trial of Exemestane +/- MM-121 in Postmenopausal Women With Locally Advanced or Metastatic Estrogen Receptor Positive and/or Progesterone Receptor Positive Her2 Negative Breast Cancer
Status: Enrolling
Updated: 3/1/2013
Rush University Medical Center
mi
from
Chicago, IL
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Her2 Negative Breast Cancer Patients Clinical Trial
Trial of Exemestane +/- MM-121 in Postmenopausal Women With Locally Advanced or Metastatic Estrogen Receptor Positive and/or Progesterone Receptor Positive Her2 Negative Breast Cancer
Status: Enrolling
Updated: 3/1/2013
Southwest Cancer Center
mi
from
Murrieta, CA
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Her2 Negative Breast Cancer Patients Clinical Trial
Trial of Exemestane +/- MM-121 in Postmenopausal Women With Locally Advanced or Metastatic Estrogen Receptor Positive and/or Progesterone Receptor Positive Her2 Negative Breast Cancer
Status: Enrolling
Updated: 3/1/2013
Wilshire Oncology Medical Group, Inc.
mi
from
Pomona, CA
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Her2 Negative Breast Cancer Patients Clinical Trial
Trial of Exemestane +/- MM-121 in Postmenopausal Women With Locally Advanced or Metastatic Estrogen Receptor Positive and/or Progesterone Receptor Positive Her2 Negative Breast Cancer
Status: Enrolling
Updated: 3/1/2013
California Pacific Cancer Center
mi
from
San Francisco, CA
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Hereditary Hemorrhagic Telangiectasia Clinical Trial
Cerebral Hemorrhage Risk in Hereditary Hemorrhagic Telangiectasia
Status: Enrolling, Phase
Updated: 12/31/1969
Augusta University
mi
from
Augusta, GA
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Hereditary Hemorrhagic Telangiectasia Clinical Trial
Cerebral Hemorrhage Risk in Hereditary Hemorrhagic Telangiectasia
Status: Enrolling, Phase
Updated: 12/31/1969
University of California at San Francisco
mi
from
San Francisco, CA
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Oncology Clinical Trial
131-I-MIBG Therapy for Refractory Neuroblastoma and Metastatic Paraganglioma/Pheochromocytoma
Status: Enrolling, Phase
Updated: 12/31/1969
Children's Hospital of Philadelphia
mi
from
Philadelphia, PA
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Hematology, Oncology Clinical Trial
INCB18424 in Treating Young Patients With Relapsed or Refractory Solid Tumor, Leukemia, or Myeloproliferative Disease
Status: Enrolling, Phase I
Updated: 1/29/2014
C.S. Mott Children's Hospital at University of Michigan Medical Center
mi
from
Ann Arbor, MI
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Hematology, Oncology Clinical Trial
INCB18424 in Treating Young Patients With Relapsed or Refractory Solid Tumor, Leukemia, or Myeloproliferative Disease
Status: Enrolling, Phase I
Updated: 1/29/2014
St. Jude Children's Research Hospital
mi
from
Memphis, TN
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Hematology, Oncology Clinical Trial
INCB18424 in Treating Young Patients With Relapsed or Refractory Solid Tumor, Leukemia, or Myeloproliferative Disease
Status: Enrolling, Phase I
Updated: 1/29/2014
Masonic Cancer Center at University of Minnesota
mi
from
Minneapolis, MN
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Hematology, Oncology Clinical Trial
INCB18424 in Treating Young Patients With Relapsed or Refractory Solid Tumor, Leukemia, or Myeloproliferative Disease
Status: Enrolling, Phase I
Updated: 1/29/2014
Children's Hospital of Philadelphia
mi
from
Philadelphia, PA
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Hematology, Oncology Clinical Trial
INCB18424 in Treating Young Patients With Relapsed or Refractory Solid Tumor, Leukemia, or Myeloproliferative Disease
Status: Enrolling, Phase I
Updated: 1/29/2014
Children's Hospital and Regional Medical Center - Seattle
mi
from
Seattle, WA
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Hematology, Oncology Clinical Trial
INCB18424 in Treating Young Patients With Relapsed or Refractory Solid Tumor, Leukemia, or Myeloproliferative Disease
Status: Enrolling, Phase I
Updated: 1/29/2014
Riley's Children Cancer Center at Riley Hospital for Children
mi
from
Indianapolis, IN
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Sinusitis Clinical Trial
Short (5 Days) Versus Long (14 Days) Duration of Antimicrobial Therapy for Acute Bacterial Sinusitis in Children
Status: Enrolling
Updated: 2/26/2016
UW Health Pediatrics (WestTowne)
mi
from
Madison, WI
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Inflammatory Bowel Disease Clinical Trial
Multi-Center African-American Inflammatory Bowel Disease Study (MAAIS)
Status: Enrolling, Phase
Updated: 12/31/1969
University of North Carolina at Chapel Hill
mi
from
Chapel Hill, NC
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Inflammatory Bowel Disease Clinical Trial
Multi-Center African-American Inflammatory Bowel Disease Study (MAAIS)
Status: Enrolling, Phase
Updated: 12/31/1969
University of Louisville
mi
from
Louisville, KY
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Celiac Disease Clinical Trial
Celiac Disease Database
Status: Enrolling
Updated: 12/2/2013
University of Chicago Medical Center
mi
from
Chicago, IL
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Oncology Clinical Trial
Dasatinib With Fludarabine and Rituximab in Relapsed and Refractory Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL)
Status: Enrolling, Phase II
Updated: 11/30/2012
Dana-Farber Cancer Institute
mi
from
Boston, MA
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Leukemia Clinical Trial
Collection of Blood and/or Bone Marrow for Investigation and Characterization of Normal and Abnormal Cell Growth
Status: Enrolling, Phase
Updated: 3/27/2018
Univ of Massachusetts Med School
mi
from
Worcester, MA
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Liver Neoplasms Clinical Trial
Intra-arterial Y-90 TheraSpheres for Hepatic Metastases From Solid Tumors
Status: Enrolling
Updated: 11/29/2012
Johns Hopkins Hospital
mi
from
Baltimore, MD
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Aging Clinical Trial
Oxidative Stress Links Aging, Activity and Mobility Limitation
Status: Enrolling, Phase I
Updated: 1/28/2016
VA Salt Lake City Health Care System, Salt Lake City, UT
mi
from
Salt Lake City, UT
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Hematology, Oncology Clinical Trial
Questionnaire and Tissue Banking For Multiple Myeloma, Waldenstrom Macroglobulinemia and Related Disorders
Status: Enrolling, Phase
Updated: 12/31/1969
Dana-Farber Cancer Institute
mi
from
Boston, MA
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Hematology Clinical Trial
A Phase III Safety and Efficacy Study of L-Glutamine to Treat Sickle Cell Disease or Sickle βo-thalassemia
Status: Enrolling
Updated: 8/31/2012
Johns Hopkins University
mi
from
Baltimore, MD
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Hematology Clinical Trial
A Phase III Safety and Efficacy Study of L-Glutamine to Treat Sickle Cell Disease or Sickle βo-thalassemia
Status: Enrolling
Updated: 8/31/2012
University of Florida
mi
from
Gainesville, FL
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Hematology Clinical Trial
A Phase III Safety and Efficacy Study of L-Glutamine to Treat Sickle Cell Disease or Sickle βo-thalassemia
Status: Enrolling
Updated: 8/31/2012
Children's Mercy Hospital
mi
from
Kansas City, MO
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Hematology Clinical Trial
A Phase III Safety and Efficacy Study of L-Glutamine to Treat Sickle Cell Disease or Sickle βo-thalassemia
Status: Enrolling
Updated: 8/31/2012
Brookdale University Hospital and Medical Center
mi
from
Brooklyn, NY
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Hematology Clinical Trial
A Phase III Safety and Efficacy Study of L-Glutamine to Treat Sickle Cell Disease or Sickle βo-thalassemia
Status: Enrolling
Updated: 8/31/2012
New York Methodist Hospital - SC/Thalassemia Program
mi
from
Brooklyn, NY
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Hematology Clinical Trial
A Phase III Safety and Efficacy Study of L-Glutamine to Treat Sickle Cell Disease or Sickle βo-thalassemia
Status: Enrolling
Updated: 8/31/2012
Presbyterian Blume Pediatric Hematology-Oncology Clinic
mi
from
Charlotte, NC
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Cardiology / Vascular Diseases Clinical Trial
The OMEGA Clinical Trial
Status: Enrolling
Updated: 7/31/2012
The Carl and Edyth Lindner Center for Research and Education at the Christ Hospital
mi
from
Cincinnati, OH
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Cardiology / Vascular Diseases Clinical Trial
The OMEGA Clinical Trial
Status: Enrolling
Updated: 7/31/2012
Riverside Methodist Hospital
mi
from
Columbus, OH
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Gastroenterology, Other, Reproductive Clinical Trial
Effect of Vitamin D Supplementation on In-vitro Fertilization (IVF) Outcomes
Status: Enrolling, Phase II
Updated: 7/24/2013
Northwestern Memorial Hospital
mi
from
Chicago, IL
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Tetralogy of Fallot Clinical Trial
Assessment of Right Ventricular Volume in Tetralogy of Fallott (TOF) Patients
Status: Enrolling
Updated: 10/5/2012
Univ of Nebraska Med Ctr
mi
from
Omaha, NE
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Hematology, Immunology / Infectious Diseases, Oncology Clinical Trial
Lenalidomide With or Without Rituximab in Treating Patients With Progressive or Relapsed Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma, Prolymphocytic Leukemia, or Non-Hodgkin Lymphoma Previously Treated With Donor Stem Cell Transplant
Status: Enrolling
Updated: 8/26/2013
Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium
mi
from
Seattle, WA
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Oncology Clinical Trial
A Study of Brentuximab Vedotin in Relapsed or Refractory Non-Hodgkin Lymphoma
Status: Enrolling, Phase II
Updated: 11/3/2014
Emory Winship Cancer Institute
mi
from
Atlanta, GA
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Oncology Clinical Trial
A Study of Brentuximab Vedotin in Relapsed or Refractory Non-Hodgkin Lymphoma
Status: Enrolling, Phase II
Updated: 11/3/2014
Medical University of South Carolina
mi
from
Charleston, SC
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Oncology Clinical Trial
A Study of Brentuximab Vedotin in Relapsed or Refractory Non-Hodgkin Lymphoma
Status: Enrolling, Phase II
Updated: 11/3/2014
M.D. Anderson Cancer Center at University of Texas
mi
from
Houston, TX
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Oncology Clinical Trial
A Study of Brentuximab Vedotin in Relapsed or Refractory Non-Hodgkin Lymphoma
Status: Enrolling, Phase II
Updated: 11/3/2014
PMK Medical Group, Inc., dba Ventura County Hematology Oncology Specialists
mi
from
Oxnard, CA
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Oncology Clinical Trial
A Study of Brentuximab Vedotin in Relapsed or Refractory Non-Hodgkin Lymphoma
Status: Enrolling, Phase II
Updated: 11/3/2014
Seattle Cancer Care Alliance/University of Washington Medical Center
mi
from
Seattle, WA
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Oncology Clinical Trial
A Study of Brentuximab Vedotin in Relapsed or Refractory Non-Hodgkin Lymphoma
Status: Enrolling, Phase II
Updated: 11/3/2014
Northwest Cancer Specialists
mi
from
Vancouver, WA
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Major Depressive Disorder Clinical Trial
Efficacy Study of Lu AA21004 on Cognitive Dysfunction in Adult Patients With Major Depressive Disorder
Status: Enrolling
Updated: 3/22/2013
US001
mi
from
National City, CA
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Major Depressive Disorder Clinical Trial
Efficacy Study of Lu AA21004 on Cognitive Dysfunction in Adult Patients With Major Depressive Disorder
Status: Enrolling
Updated: 3/22/2013
US011
mi
from
New York, NY
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Endocrinology, Oncology, Reproductive Clinical Trial
Effect of Metformin on Adrenal or Ovarian Androgen Production in Overweight Pubertal Girls With Androgen Excess
Status: Enrolling
Updated: 1/19/2018
University of Virginia Center for Research in Reproduction
mi
from
Charlottesville, VA
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Endocrinology, Oncology, Reproductive Clinical Trial
Effect of Spironolactone on Adrenal or Ovarian Androgen Production in Overweight Pubertal Girls With Androgen Excess
Status: Enrolling
Updated: 1/19/2018
University of Virginia Center for Research in Reproduction
mi
from
Charlottesville, VA
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Infection Clinical Trial
Antibiotic Prophylaxis Before Percutaneous Gastrostomy
Status: Enrolling
Updated: 12/3/2015
Harborview Medical Center
mi
from
Seattle, WA
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Psychiatry / Psychology, Pulmonary / Respiratory Diseases Clinical Trial
Brain Circuits in Schizophrenia and Smoking
Status: Enrolling, Phase
Updated: 12/31/1969
Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicine
mi
from
Baltimore, MD
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Rheumatology Clinical Trial
The Pathogenesis and Natural History of Sjogren s Syndrome
Status: Enrolling, Phase
Updated: 12/31/1969
National Institutes of Health Clinical Center, 9000 Rockville Pike
mi
from
Bethesda, MD
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Immunology / Infectious Diseases, Pulmonary / Respiratory Diseases Clinical Trial
Vitamin D for Enhancing the Immune System in Cystic Fibrosis (DISC Study)
Status: Enrolling, Phase III
Updated: 12/16/2015
University of Alabama at Birmingham
mi
from
Birmingham, AL
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Immunology / Infectious Diseases, Pulmonary / Respiratory Diseases Clinical Trial
Vitamin D for Enhancing the Immune System in Cystic Fibrosis (DISC Study)
Status: Enrolling, Phase III
Updated: 12/16/2015
University of Iowa
mi
from
Iowa City, IA
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Immunology / Infectious Diseases, Pulmonary / Respiratory Diseases Clinical Trial
Vitamin D for Enhancing the Immune System in Cystic Fibrosis (DISC Study)
Status: Enrolling, Phase III
Updated: 12/16/2015
Emory Hospital
mi
from
Atlanta, GA
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Immunology / Infectious Diseases, Pulmonary / Respiratory Diseases Clinical Trial
Vitamin D for Enhancing the Immune System in Cystic Fibrosis (DISC Study)
Status: Enrolling, Phase III
Updated: 12/16/2015
University of Cincinnati
mi
from
Cincinnati, OH
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Immunology / Infectious Diseases, Pulmonary / Respiratory Diseases Clinical Trial
Vitamin D for Enhancing the Immune System in Cystic Fibrosis (DISC Study)
Status: Enrolling, Phase III
Updated: 12/16/2015
Case Western Reserve Univ
mi
from
Cleveland, OH
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Hematology, Oncology Clinical Trial
Dasatinib and Cyclosporine in Treating Patients With Chronic Myelogenous Leukemia Refractory or Intolerant to Imatinib Mesylate
Status: Enrolling
Updated: 7/1/2013
University of Colorado Cancer Center - Anschutz Cancer Pavilion
mi
from
Aurora, CO
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Hepatitis C Virus Clinical Trial
Study With PegInterferon Alfa-2a, Ribavirin and BMS-790052 With or Without BMS-650032 for Participants in Some Hepatitis C Virus (HCV) Trials
Status: Enrolling, Phase II
Updated: 12/2/2013
University of Miami
mi
from
Miami, FL
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Hepatitis C Virus Clinical Trial
Study With PegInterferon Alfa-2a, Ribavirin and BMS-790052 With or Without BMS-650032 for Participants in Some Hepatitis C Virus (HCV) Trials
Status: Enrolling, Phase II
Updated: 12/2/2013
Mercy Medical Center
mi
from
Baltimore, MD
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Hepatitis C Virus Clinical Trial
Study With PegInterferon Alfa-2a, Ribavirin and BMS-790052 With or Without BMS-650032 for Participants in Some Hepatitis C Virus (HCV) Trials
Status: Enrolling, Phase II
Updated: 12/2/2013
Uf Hepatology Research At Ctrb
mi
from
Gainesville, FL
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Hepatitis C Virus Clinical Trial
Study With PegInterferon Alfa-2a, Ribavirin and BMS-790052 With or Without BMS-650032 for Participants in Some Hepatitis C Virus (HCV) Trials
Status: Enrolling, Phase II
Updated: 12/2/2013
North Shore Long Island Jewish Health System
mi
from
Manhasset, NY
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Hepatitis C Virus Clinical Trial
Study With PegInterferon Alfa-2a, Ribavirin and BMS-790052 With or Without BMS-650032 for Participants in Some Hepatitis C Virus (HCV) Trials
Status: Enrolling, Phase II
Updated: 12/2/2013
Washington University School of Medicine
mi
from
Saint Louis, MO
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Non-24-Hour Sleep-Wake Disorder Clinical Trial
Tasimelteon for the Treatment of Non-24-hour Sleep-Wake Disorder (N24HSWD) in Blind Individuals With no Light Perception
Status: Enrolling, Phase III
Updated: 12/9/2014
The Center for Sleep and Wake Disorders (Washington, D.C. Metropolitan Area)
mi
from
Chevy Chase, MD
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Non-24-Hour Sleep-Wake Disorder Clinical Trial
Tasimelteon for the Treatment of Non-24-hour Sleep-Wake Disorder (N24HSWD) in Blind Individuals With no Light Perception
Status: Enrolling, Phase III
Updated: 12/9/2014
Todd J. Swick, MD, PA
mi
from
Houston, TX
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Non-24-Hour Sleep-Wake Disorder Clinical Trial
Tasimelteon for the Treatment of Non-24-hour Sleep-Wake Disorder (N24HSWD) in Blind Individuals With no Light Perception
Status: Enrolling, Phase III
Updated: 12/9/2014
Kendall South Medical Center, Inc.
mi
from
Miami, FL
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Non-24-Hour Sleep-Wake Disorder Clinical Trial
Tasimelteon for the Treatment of Non-24-hour Sleep-Wake Disorder (N24HSWD) in Blind Individuals With no Light Perception
Status: Enrolling, Phase III
Updated: 12/9/2014
VA Palo Alto Health Care System/PAIRE (San Fransisco Bay Area)
mi
from
Palo Alto, CA
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Non-24-Hour Sleep-Wake Disorder Clinical Trial
Tasimelteon for the Treatment of Non-24-hour Sleep-Wake Disorder (N24HSWD) in Blind Individuals With no Light Perception
Status: Enrolling, Phase III
Updated: 12/9/2014
Consolidated Clinical trials
mi
from
Pittsburgh, PA
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Non-24-Hour Sleep-Wake Disorder Clinical Trial
Tasimelteon for the Treatment of Non-24-hour Sleep-Wake Disorder (N24HSWD) in Blind Individuals With no Light Perception
Status: Enrolling, Phase III
Updated: 12/9/2014
Columbia Research Group Inc.
mi
from
Portland, OR
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Ischemic Stroke Clinical Trial
Assess the Penumbra System in the Treatment of Acute Stroke
Status: Enrolling, Phase IV
Updated: 2/19/2014
Endovascular Surgical Neuroradiology, Swedish Medical Center
mi
from
Denver, CO
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Ischemic Stroke Clinical Trial
Assess the Penumbra System in the Treatment of Acute Stroke
Status: Enrolling, Phase IV
Updated: 2/19/2014
Medical College of Wisconsin
mi
from
Milwaukee, WI
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Other Clinical Trial
Specimen Collection From Pregnant Women at Increased Risk for Fetal Aneuploidy
Status: Enrolling
Updated: 4/18/2016
Henry Ford Hospital
mi
from
Detroit, MI
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Other Clinical Trial
Specimen Collection From Pregnant Women at Increased Risk for Fetal Aneuploidy
Status: Enrolling
Updated: 4/18/2016
Spectrum Health
mi
from
Grand Rapids, MI
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Other Clinical Trial
Specimen Collection From Pregnant Women at Increased Risk for Fetal Aneuploidy
Status: Enrolling
Updated: 4/18/2016
Sharp Rees-Stealy Medical Group, Inc.
mi
from
San Diego, CA
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Other Clinical Trial
Specimen Collection From Pregnant Women at Increased Risk for Fetal Aneuploidy
Status: Enrolling
Updated: 4/18/2016
Specialty Obstetrics of San Diego
mi
from
San Diego, CA
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Oncology Clinical Trial
In Vitro Expanded Allogeneic Epstein-Barr Virus Specific Cytotoxic T-Lymphocytes (EBV-CTLs) Genetically Targeted to the CD19 Antigen in B-cell Malignancies
Status: Enrolling, Phase I
Updated: 4/30/2018
Memorial Sloan-Kettering Cancer Center 1275 York Avenue
mi
from
New York, NY
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Non-24-Hour Sleep-Wake Disorder Clinical Trial
Withdrawal Study to Demonstrate the Maintenance Effect in the Treatment of Non-24-Hour Sleep-Wake Disorder
Status: Enrolling
Updated: 1/25/2012
The Center for Sleep and Wake Disorders (Washington, D.C. Metropolitan Area)
mi
from
Chevy Chase, MD
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Non-24-Hour Sleep-Wake Disorder Clinical Trial
Withdrawal Study to Demonstrate the Maintenance Effect in the Treatment of Non-24-Hour Sleep-Wake Disorder
Status: Enrolling
Updated: 1/25/2012
Todd J. Swick, MD, PA
mi
from
Houston, TX
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Non-24-Hour Sleep-Wake Disorder Clinical Trial
Withdrawal Study to Demonstrate the Maintenance Effect in the Treatment of Non-24-Hour Sleep-Wake Disorder
Status: Enrolling
Updated: 1/25/2012
Kendall South Medical Center, Inc.
mi
from
Miami, FL
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Non-24-Hour Sleep-Wake Disorder Clinical Trial
Withdrawal Study to Demonstrate the Maintenance Effect in the Treatment of Non-24-Hour Sleep-Wake Disorder
Status: Enrolling
Updated: 1/25/2012
VA Palo Alto Health Care System/PAIRE (San Fransisco Bay Area)
mi
from
Palo Alto, CA
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Non-24-Hour Sleep-Wake Disorder Clinical Trial
Withdrawal Study to Demonstrate the Maintenance Effect in the Treatment of Non-24-Hour Sleep-Wake Disorder
Status: Enrolling
Updated: 1/25/2012
Consolidated Clinical trials
mi
from
Pittsburgh, PA
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Non-24-Hour Sleep-Wake Disorder Clinical Trial
Withdrawal Study to Demonstrate the Maintenance Effect in the Treatment of Non-24-Hour Sleep-Wake Disorder
Status: Enrolling
Updated: 1/25/2012
Columbia Research Group Inc.
mi
from
Portland, OR
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Cardiology / Vascular Diseases, Psychiatry / Psychology, Pulmonary / Respiratory Diseases Clinical Trial
Effects of Nocturnal Nasal Oxygen on Biomarkers in Sleep Apnea Patients With Heart Failure
Status: Enrolling
Updated: 5/11/2012
University of Maryland
mi
from
Baltimore, MD
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Cardiology / Vascular Diseases, Psychiatry / Psychology, Pulmonary / Respiratory Diseases Clinical Trial
Effects of Nocturnal Nasal Oxygen on Biomarkers in Sleep Apnea Patients With Heart Failure
Status: Enrolling
Updated: 5/11/2012
Baltimore VA Medical Center
mi
from
Baltimore, MD
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Pulmonary Disease, Chronic Obstructive Clinical Trial
Tiotropium +Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD)
Status: Enrolling
Updated: 10/17/2012
205.452.01130 Boehringer Ingelheim Investigational Site
mi
from
Atlanta, GA
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Pulmonary Disease, Chronic Obstructive Clinical Trial
Tiotropium +Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD)
Status: Enrolling
Updated: 10/17/2012
Boehringer Ingelheim Investigational Site
mi
from
Charlotte, NC
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Pulmonary Disease, Chronic Obstructive Clinical Trial
Tiotropium +Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD)
Status: Enrolling
Updated: 10/17/2012
205.452.01199 Boehringer Ingelheim Investigational Site
mi
from
Danbury, CT
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Pulmonary Disease, Chronic Obstructive Clinical Trial
Tiotropium +Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD)
Status: Enrolling
Updated: 10/17/2012
205.452.01279 Boehringer Ingelheim Investigational Site
mi
from
Great Neck, NY
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Pulmonary Disease, Chronic Obstructive Clinical Trial
Tiotropium +Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD)
Status: Enrolling
Updated: 10/17/2012
Boehringer Ingelheim Investigational Site
mi
from
Greenville, SC
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Pulmonary Disease, Chronic Obstructive Clinical Trial
Tiotropium +Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD)
Status: Enrolling
Updated: 10/17/2012
1199.14.1083 Boehringer Ingelheim Investigational Site
mi
from
Henderson, NV
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Pulmonary Disease, Chronic Obstructive Clinical Trial
Tiotropium +Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD)
Status: Enrolling
Updated: 10/17/2012
Boehringer Ingelheim Investigational Site
mi
from
Philadelphia, PA
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Cardiology / Vascular Diseases, Dermatology / Plastic Surgery, Endocrinology, Gastroenterology, Hematology, Immunology / Infectious Diseases, Musculoskeletal, Nephrology / Urology, Neurology, Ophthalmology, Otolaryngology, Psychiatry / Psychology, Pulmonary / Respiratory Diseases, Other Clinical Trial
Pharmacokinetics of Understudied Drugs Administered to Children Per Standard of Care
Status: Enrolling, Phase
Updated: 4/2/2018
University of Mississippi Medical Center
mi
from
Jackson, MS
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Cardiology / Vascular Diseases, Dermatology / Plastic Surgery, Endocrinology, Gastroenterology, Hematology, Immunology / Infectious Diseases, Musculoskeletal, Nephrology / Urology, Neurology, Ophthalmology, Otolaryngology, Psychiatry / Psychology, Pulmonary / Respiratory Diseases, Other Clinical Trial
Pharmacokinetics of Understudied Drugs Administered to Children Per Standard of Care
Status: Enrolling, Phase
Updated: 4/2/2018
University of New Mexico Health Sciences Center
mi
from
Albuquerque, NM
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Cardiology / Vascular Diseases, Dermatology / Plastic Surgery, Endocrinology, Gastroenterology, Hematology, Immunology / Infectious Diseases, Musculoskeletal, Nephrology / Urology, Neurology, Ophthalmology, Otolaryngology, Psychiatry / Psychology, Pulmonary / Respiratory Diseases, Other Clinical Trial
Pharmacokinetics of Understudied Drugs Administered to Children Per Standard of Care
Status: Enrolling, Phase
Updated: 4/2/2018
University of Vermont Medical Center
mi
from
Burlington, VT
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Cardiology / Vascular Diseases, Dermatology / Plastic Surgery, Endocrinology, Gastroenterology, Hematology, Immunology / Infectious Diseases, Musculoskeletal, Nephrology / Urology, Neurology, Ophthalmology, Otolaryngology, Psychiatry / Psychology, Pulmonary / Respiratory Diseases, Other Clinical Trial
Pharmacokinetics of Understudied Drugs Administered to Children Per Standard of Care
Status: Enrolling, Phase
Updated: 4/2/2018
Axis Clinical Trials
mi
from
Los Angeles, CA
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Cardiology / Vascular Diseases, Dermatology / Plastic Surgery, Endocrinology, Gastroenterology, Hematology, Immunology / Infectious Diseases, Musculoskeletal, Nephrology / Urology, Neurology, Ophthalmology, Otolaryngology, Psychiatry / Psychology, Pulmonary / Respiratory Diseases, Other Clinical Trial
Pharmacokinetics of Understudied Drugs Administered to Children Per Standard of Care
Status: Enrolling, Phase
Updated: 4/2/2018
University of Montana
mi
from
Missoula, MT
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Cardiology / Vascular Diseases, Dermatology / Plastic Surgery, Endocrinology, Gastroenterology, Hematology, Immunology / Infectious Diseases, Musculoskeletal, Nephrology / Urology, Neurology, Ophthalmology, Otolaryngology, Psychiatry / Psychology, Pulmonary / Respiratory Diseases, Other Clinical Trial
Pharmacokinetics of Understudied Drugs Administered to Children Per Standard of Care
Status: Enrolling, Phase
Updated: 4/2/2018
University of Utah Hospitals and Clinics
mi
from
Salt Lake City, UT
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Hypoactive Sexual Desire Disorder Clinical Trial
Lybrido for Female Sexual Dysfunction
Status: Enrolling
Updated: 9/26/2011
Meridien Research
mi
from
St Petersburg, FL
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Hypoactive Sexual Desire Disorder Clinical Trial
Lybrido for Female Sexual Dysfunction
Status: Enrolling
Updated: 9/26/2011
Philadelphia Clinical Research
mi
from
Philadelphia, PA
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