Search clinical trials for: Oral Treprostinil

Total 8332 results

United Therapeutics
University of California, Los Angeles; Emory University; Brigham and Women's... and other collaborators

Completed

A Study to Assess the Safety and Efficacy of Treprostinil to Facilitate Liver Transplantation in Patients With Portopulmonary Hypertension

Pulmonary Arterial Hypertension | Pulmonary Hypertension | Portopulmonary Hypertension

United States
United Therapeutics

Completed

Remodulin® to Oral Treprostinil Transition

Pulmonary Arterial Hypertension

United States
Stanford University
Northwestern University

Completed

A 48-week Study of the Effect of Dual Therapy (Inhaled Treprostinil and Tadafafil) Versus Monotherapy (Tadalafil).

Hypertension, Pulmonary

United States
Stanford University

Terminated

Perioperative Treprostinil in Pediatric Patients Undergoing the Fontan Operation

Single Ventricle

United States
Hospices Civils de Lyon

Terminated

Peripheral and Coronary Endothelial Dysfunction In Type 2diabetic Patients- Role of Metformin

Coronary and Peripheral Endothelial Dysfunction

France
Rhode Island Hospital
United Therapeutics; University of Rhode Island

Recruiting

Safety and Efficacy of Treprostinil (Remodulin®) In Reducing Ischemia-Reperfusion Injury During Kidney Transplantation

Ischemia Reperfusion Injury | Delayed Graft Function

United States
Abhinav Humar, MD

Completed

Safety and Efficacy of Treprostinil in Ischemia and Reperfusion Injury in Adult Orthotopic Liver Transplantation

Ischemia Reperfusion Injury

United States
Lundquist Institute for Biomedical Innovation at...
United Therapeutics

Completed

Transition From Injectable Prostacyclin Medication to Inhaled Prostacyclin Medication

Pulmonary Arterial Hypertension

United States
Mayo Clinic
United Therapeutics

Enrolling by invitation

A Study of Treprostinil to Treat Interstitial Lung Disease Pulmonary Hypertension

Pulmonary Arterial Hypertension | Interstitial Lung Disease | Healthy Adults

United States
Children's Hospital Medical Center, Cincinnati

Terminated

Acute Effects of Inhaled Treprostinil in Fontan Patients

Congenital Heart Disease

United States
United Therapeutics

Active, not recruiting

Evaluate Real-World Use of Next Generation Infusion Pumps to Administer Remodulin (EVOLVE)

Pulmonary Arterial Hypertension

United States
Medtronic Cardiac Rhythm and Heart Failure
United Therapeutics

Active, not recruiting

DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study (DelIVery)

Pulmonary Arterial Hypertension

United States
Eunice Kennedy Shriver National Institute of Child...

Terminated

Treatment of Menorrhagia in Women With Thrombocytopenia Using Platelets or Platelets and Hormones

Amenorrhea | Aplastic Anemia | Menorrhagia

United States
Eli Lilly and Company

Completed

A Study of Treprostinil and a New Formulation of LY900014 in Healthy Japanese Participants

Healthy

Japan
United Therapeutics

Withdrawn

FREEDOM DR: Oral Treprostinil in Combination With an Endothelin Receptor Antagonist (ERA) and/or a Phosphodiesterase-5 (PDE-5) Inhibitor or as Monotherapy for the Treatment of Pulmonary Arterial Hypertension (PAH)

Pulmonary Hypertension

United States, Australia, Mexico
Burnasyan Federal Medical Biophysical Center

Completed

Clinical Study of Medicinal Product Cardionat® Using in Health Athlete Volunteers

Angina Pectoris | Stroke, Not Specified as Hemorrhage or Infarction

Russian Federation
United Therapeutics

Terminated

Remodulin as Add-on Therapy for the Treatment of Persistent Pulmonary Hypertension of the Newborn

Persistent Pulmonary Hypertension of the Newborn

United States
Purdue University

Active, not recruiting

Cephalic Phase Responses to Nutritive and Non-Nutritive Sweeteners

Pre Diabetes

United States
Université de Montréal
St. Justine's Hospital

Terminated

Comparison of Two Oral Myofunctional Reeducation Methods for Children With Obstructive Sleep Apnea (PERSIST-B)

Obstructive Sleep Apnea

Canada
Estetra
ICON Clinical Research

Completed

Estetrol for the Treatment of Moderate to Severe Vasomotor Symptoms in Postmenopausal Women (E4Comfort)

Vasomotor Symptoms | Menopausal Symptoms

United States, Canada
Pulmagen Therapeutics

Completed

A Study to Evaluate Safety, Tolerability and Pharmacokinetics of ADC3680B in Subjects With Partly Controlled Atopic Asthma

Atopic Asthma

United Kingdom
Turning Point Therapeutics, Inc.

Recruiting

A Study of Repotrectinib in Pediatric and Young Adult Subjects Harboring ALK, ROS1, OR NTRK1-3 Alterations

Lymphoma | Locally Advanced Solid Tumors | Metastatic Solid Tumors | Primary CNS Tumors

United States, Korea, Republic of, Spain, Singapore, Taiwan, Australia, Italy, Canada, France, Denmark, United Kingdom
Mansoura University

Completed

Clinical Impacts of Oral Gastrografin Follow Through in Adhesive Small Bowel Obstruction (SBO)

Small Bowel Obstruction

Egypt
German Institute of Human Nutrition
Ludwig-Maximilians - University of Munich

Completed

Immediate and Long-term Induction of Incretin Release by Artificial Sweeteners 1 (ILIAS-1)

Diabetes | Pre-diabetes

Germany
Applied Molecular Transport

Active, not recruiting

Study of the Efficacy and Safety of AMT-101 in Subjects With Ulcerative Colitis (LOMBARD)

Ulcerative Colitis

United States, Hungary, Ukraine, Germany, United Kingdom, Belarus, Bulgaria, Canada, France, Georgia, Moldova, Republic of, Poland, Russian Federation, Switzerland
Brigham and Women's Hospital

Completed

Characterizing Upper Airway Collapse to Guide Patient Selection for Oral Appliance Therapy for Obstructive Sleep Apnea

Sleep Apnea, Obstructive

United States
Wockhardt

Completed

Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple Ascending Doses of Oral WCK 2349

Pharmacokinetics
Mayo Clinic
National Center for Advancing Translational Sciences (NCATS)

Completed

MPO Inhibitor A_Zeneca for HFpEF

Heart Failure

United States
Ain Shams University

Completed

Early Versus Traditional Oral Hydration After Cesarean Section

Gastrointestinal Motility and Defecation Conditions

Egypt
EicOsis Human Health Inc.

Recruiting

Safety, Tolerability, and Pharmacokinetics of Multiple Doses of Oral EC5026 in Healthy Subjects

Healthy Subjects

New Zealand
Loma Linda University

Completed

Oral Sucrose Versus Glucose for Procedural Pain in Premature Neonates

Neonatal Procedural Pain

United States
Brigham and Women's Hospital

Completed

DAW1033D in Obstructive Sleep Apnea (OSAstimD)

Obstructive Sleep Apnea (OSA)

United States
Ain Shams Maternity Hospital

Completed

Early Versus Late Hydration After Cesarean Section (CS)

Gastrointestinal Motility and Defaecation Conditions

Egypt
The University of Hong Kong

Unknown

Treatment of Sleep Apnea With Oral Appliances

Obstructive Sleep Apnea

Hong Kong
Yonsei University

Completed

Gender and Proper Size of Oropharyngeal Airway: Pilot Study

Adult Patients Undergoing Surgery That Requires General Anesthesia

Korea, Republic of
Cara Therapeutics, Inc.

Completed

A Study to Evaluate the Safety and Efficacy of CR845 in Chronic Kidney Disease Patients With Moderate-to-Severe Pruritus

Chronic Kidney Diseases | Pruritus

United States
Johns Hopkins University
Canopy Growth Corporation

Recruiting

Pharmacokinetics and Pharmacodynamics of CHI-914 in Healthy Participants

Behavioral Pharmacology of Cannabis

United States
Vanda Pharmaceuticals

Completed

Bioequivalence Study Between Tasimelteon Capsule Formulation and Liquid Suspension Formulation in Healthy Volunteers

Healthy

United States
Harmony Biosciences, LLC

Active, not recruiting

Safety and Efficacy of Pitolisant on Excessive Daytime Sleepiness and Other Non-Muscular Symptoms in Patients With Myotonic Dystrophy Type 1

Myotonic Dystrophy 1 | Excessive Daytime Sleepiness

United States, Canada
Syntrix Biosystems, Inc.
National Institute on Drug Abuse (NIDA); DF/Net Research

Completed

Omnitram Safety and Efficacy in the Treatment of Diabetic Neuropathy

Diabetic Neuropathies | Neuropathic Pain | Pain, Chronic

United States
Segi University

Completed

Oral Stereognosis in Completely Edentulous Patient With Maxillary Tori

Torus Palatinus and Torus Mandibularis

Malaysia
Aelis Farma
National Institute on Drug Abuse (NIDA)

Completed

Multiple Ascending Dose to Study the Safety, Tolerability, PK and PD Effects of AEF0117

Healthy Volunteers

United States
Lithuanian University of Health Sciences
Klaipėda University; Vita Longa Clinic

Completed

Faringomoss Effectiveness in Inhibiting Acute Throat Pain and Discomfort

Mouth Diseases | Throat Pain | Spraying Behavior | Throat Diseases

Lithuania
St. Joseph's Hospital and Medical Center, Phoenix
Lund University

Completed

Effects of Oral Care in the Neuroscience ICU

Oral Hygiene | Ventilator Associated Pneumonia

United States
EicOsis Human Health Inc.

Recruiting

Novel Soluble Epoxide Hydrolase Inhibitor for Neuropathic Pain in Patients With Spinal Cord Injury

Neuropathic Pain | Spinal Cord Injuries

United States
Paolone Gaetano

Not yet recruiting

Study on the Chromatic Perception of Digital Systems in Aesthetic Field

Color Detection of Upper Central Incisors

Italy
Integrative Skin Science and Research
Vidya Herbs (Sponsor)

Recruiting

The Effects of an Oral Hair Supplement on Hair Density, Growth, and Microbiome

Hair Thinning

United States
Fulcrum Therapeutics

Terminated

Losmapimod Safety and Efficacy in COVID-19 (LOSVID)

COVID-19

United States, Mexico, Brazil, Peru
Universidad de Almeria

Enrolling by invitation

Physiotherapy to Improve Feeding Skills in Preterm Infants

Premature Birth | Neurodevelopmental Disorders | Motor Disorders | Parenteral Nutrition | Sucking Behavior

Spain
EicOsis Human Health Inc.

Completed

Safety, Tolerability, Pharmacokinetics and Food Effects of Oral EC5026 in Healthy Subjects

Healthy Adults

United States

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