Search clinical trials for: oral and IV ramosetron

Total 9850 results

Seoul National University Bundang Hospital

Unknown

The Effect of Oral and Intravenous Ramosetron During Laparoscopic Cholecystectomy

Nausea | Vomiting | Laparoscopic Cholecystectomy

Korea, Republic of
Thammasat University

Completed

Effect of Ramosetron in Prevention of Intrathecal Morphine Induced Nausea and Vomiting

Postoperative Nausea and Vomiting
Yonsei University

Completed

Dose-ranging Study of Ramosetron for the Prevention of Nausea and Vomiting After Gynecologic Laparoscopic Surgery

Postoperative Nausea and Vomiting

Korea, Republic of
Thammasat University Hospital

Recruiting

Oral Fluid vs IV Fluid After Primary TKA

Osteoarthritis, Knee | Total Knee Arthroplasty | Oral Fluid Replacement

Thailand
Hoffmann-La Roche

Completed

A Study Investigating the Absolute Oral Bioavailability of Balovaptan After Single and Multiple Daily Oral Doses of Balovaptan in Healthy Volunteers

Healthy Volunteers

Netherlands
Pediatrix
Banner Health

Terminated

Hydrotherapy for the Reversal of Oligohydramnios (STRONG)

Oligohydramnios

United States
Wockhardt

Completed

Phase I, Open Label,Crossover Food-Effect and Absolute Bioavailability Study of WCK2349 and WCK771 in Healthy Adult Human Volunteers

Effect of Food

United States
Chonnam National University Hospital

Completed

Phamacokinetic and Pharmacodynamic Study of Ramosetron in Chemotherapy Induced Nasea and Vomiting

Colon Cancer

Korea, Republic of
GlaxoSmithKline

Completed

A Study to Investigate the Safety, Tolerability and Pharmacokinetics of Oral and Intravenous GSK1322322 in Healthy Subjects

Infections, Bacterial

United States
Prana Biotechnology Limited

Completed

Absorption, Metabolism and Excretion Study of [14C]PBT2 and Absolute Bioavailability of PBT2

Healthy Volunteers

United Kingdom
GlaxoSmithKline

Completed

Part A: Radiolabel Study With GW786034 Part B: Single Dose of GW786034

Carcinoma, Renal Cell

United States
Pfizer

Completed

A Study to Understand How the Study Medicine (PF-07081532) is Processed and Eliminated in Healthy Men

Healthy Participants

Netherlands
Pfizer

Completed

A Study in Healthy Adult Male Participants to Assess Absorption, Distribution, Metabolism and Excretion (ADME) of Radiolabeled PF-06865571.

Healthy Participants

United States
Syros Pharmaceuticals

Suspended

A Study for Oral SY-2101 for Participants With Acute Promyelocytic Leukemia

Acute Promyelocytic Leukemia

United States
Pfizer

Active, not recruiting

A Study to Understand What the Body Does to the Study Medicine Called PF-07220060 When Taken by Healthy Adults

Healthy Participants

Netherlands
Aquinox Pharmaceuticals (Canada) Inc.
Quotient Clinical

Completed

Phase 1 Absorption Distribution Metabolism and Excretion of AQX-1125 (ADME)

Healthy Volunteer

United Kingdom
Theravance Biopharma

Completed

TD-1473 Absorption, Distribution, Metabolism and Excretion (ADME) Study in Healthy Male Subjects

Bowel Diseases, Inflammatory | Intestinal Disorders

United States
Genentech, Inc.

Completed

An Absolute Bioavailability Study in Healthy Participants Comparing Oral to Intravenous Administration of GDC-0973 (Cobimetinib)

Healthy Volunteers
Neurocrine Biosciences
Takeda

Completed

A Study to Assess Absolute Bioavailability (ABA) of TAK-831 and to Characterize Mass Balance, Pharmacokinetics (PK), Metabolism, and Excretion of [14C]TAK-831 in Male Healthy Participants

Healthy Volunteers

United States
Pusan National University Yangsan Hospital
Korean Medicine Hospital of Pusan National University; Korea Institute of Oriental...

Completed

Acupuncture for Postoperative Nausea and Vomiting in Patients Undergoing Colorectal Surgery (AcuPONV)

Colorectal Neoplasms | Postoperative Nausea and Vomiting

Korea, Republic of
Pfizer

Completed

Glasdegib Absolute Bioavailability Study

Healthy Volunteer Study

United States
Boehringer Ingelheim

Completed

Pharmacokinetics of Talsaclidine After Administration to Healthy Subjects

Healthy
Odense University Hospital
Novo Nordisk A/S; Department of Nephrology, Odense University Hospital; The A... and other collaborators

Recruiting

Intravenous vs. Oral Hydration to Reduce the Risk of Post-Contrast Acute Kidney Injury After Intravenous Contrast-Enhanced Computed Tomography in Patients With Severe Chronic Kidney Disease (ENRICH)

Kidney Failure, Chronic | Kidney Injury | Risk Reduction | Contrast-induced Nephropathy

Denmark
Imam Khomeini Hospital
Tehran Heart Center

Unknown

N-Acetyl Cystein and Contrast Nephropathy

Radiographic Contrast Agent Nephropathy | Chronic Kidney Disease Stage 2

Iran, Islamic Republic of
Murdoch Childrens Research Institute

Recruiting

BonE and Joint Infections - Simplifying Treatment in Children Trial (BEST)

Osteomyelitis | Septic Arthritis | Bone Infection | Bone and Joint Infection

New Zealand, Australia
Genentech, Inc.

Completed

A Study of the Hedgehog Pathway Inhibitor GDC-0449 in Healthy Female Subjects of Non-Childbearing Potential

Healthy
Galera Therapeutics, Inc.

Completed

A Phase 1 Study of the Safety and Pharmacokinetics of GC4711 (Oral Capsule) Compared to GC4419 (IV Infusion) and GC4711 (IV Infusion) in Healthy Volunteers

Healthy Volunteers

Australia
The Catholic University of Korea

Unknown

Efficacy Study of Ramosetron in the Setting of Hematopoietic Stem Cell Transplantation

Hematologic Malignancies

Korea, Republic of
Pusan National University Hospital

Completed

Ramosetron on Late PONV (Postoperative Nausea and Vomiting)

Postoperative Nausea and Vomiting | Breast Cancer Female

Korea, Republic of
Milton S. Hershey Medical Center

Terminated

Clinical, Pharmacological and Molecular Effects of IV and Oral Acetaminophen in Adults With aSAH (aSAH)

Stroke | Subarachnoid Hemorrhage

United States
Janssen Pharmaceutical K.K.

Completed

A Pharmacokinetic Study of JK1211(Itraconazole [Itrizole]) Oral Solution in Participants With Deep Mycosis and Those With Febrile Neutropenia Suspected of Fungal Infection

Mycoses | Candidiasis | Neutropenia | Aspergillosis | Cryptococcosis | Histoplasmosis | Blastomycosis

Japan
Astellas Pharma Inc

Completed

A Study to Assess the Efficacy and Safety of YM060 in Female Patients With Diarrhea-predominant Irritable Bowel Syndrome (IBS)

Diarrhea-predominant Irritable Bowel Syndrome

Japan
Astellas Pharma Inc

Completed

A Study to Compare Oral Absorption of YM060 Between Orally-disintegrating Tablet (Without Water) and Conventional Tablet

Healthy | Plasma Concentration of YM060

Japan
Yonsei University

Completed

Efficacy of Dexamethasone Added to Ramosetron for Preventing Postoperative Nausea and Vomiting in Highly Susceptible Patients Following Spine Surgery

Nausea | Vomiting
University of Nebraska

Completed

The Prospective Evaluation of Pancreatic Function in Pancreas Transplant Recipients

Diabetes | Transplant

United States
Nicklaus Children's Hospital f/k/a Miami Children...
Einsoff Biohealth

Terminated

Comparing Speedlyte and IV Rehydration Treating Children With Gastroenteritis in a Pediatric Emergency Department (ED)

Dehydration | Acute Gastroenteritis

United States
GlaxoSmithKline

Terminated

A Positron Emission Tomography (PET) Study to Investigate the Brain Biodistribution of 18F GSK2647544 in Healthy Subjects to Determine Its Ability to Cross the Blood-brain-barrier.

Alzheimer's Disease

United Kingdom
Astellas Pharma Inc

Completed

A Study to Compare Oral Absorption of YM060 Between Orally-disintegrating Tablet and Conventional Tablet Under With Water Intake

Healthy | Plasma Concentration of YM060

Japan
Mallinckrodt

Completed

Drug Interactions Between Morphine and Orally or IV Administered Acetaminophen

Pain

United States
Takeda

Completed

Study to Assess Absolute Bioavailability of TAK-935 (OV935) and to Characterize Mass Balance, Pharmacokinetics, Metabolism, and Excretion of [14C]TAK-935 (OV935) in Healthy Male Participants

Healthy Volunteers

United States
Astellas Pharma Inc

Completed

A Study to Evaluate Efficacy of YM060 on Diarrhea-predominant Irritable Bowel Syndrome (D-IBS) in Female Patients

Irritable Bowel Syndrome

Japan
University Health Network, Toronto

Not yet recruiting

Intravenous vs Oral Acetaminophen in Postoperative Hip Fracture Adult Patients (INTACT-HIP)

Surgery | Hip-fracture
F2G Biotech GmbH
Quotient Clinical

Withdrawn

Radiolabelled IV and Oral Metabolism Study of F901318 (ADME)

Invasive Aspergillosis

United Kingdom
National Institute on Alcohol Abuse and Alcoholism...

Completed

Dopaminergic Modulation of Brain Activation Using Simultaneous PET/Pharmacological MRI

Normal Physiology

United States
Assistance Publique - Hôpitaux de Paris

Completed

Oral Versus Intravenous Rehydration for Prevention of Dehydration in Premature Babies, During the First Days of Life. (SROPREMA)

Enteral Nutrition | Low Birth Weight Infant

France
UCB Pharma

Completed

A Trial to Investigate the Safety, Tolerability and Pharmacokinetics of Intravenous SPM 927

Epilepsy
Kelowna General Hospital
Capital Health, Canada; Canadian Society of Hospital Pharmacists; Interior Health...

Completed

Comparison of Intravenous Cefazolin Plus Oral Probenecid With Oral Cephalexin for the Treatment of Cellulitis

Cellulitis

Canada
Debiopharm International SA

Completed

A Study to Evaluate the Absorption, Metabolism, and Excretion and Absolute Bioavailability of Xevinapant in Healthy Male Participants

Healthy Volunteers

United Kingdom
Konkuk University Medical Center

Completed

Ramosetron Pre-treatment for PONV and QT Prolongation

PONV | Prolonged QTc Interval

Korea, Republic of
University of Wisconsin, Madison
TRYP Therapeutics

Withdrawn

Bioavailability Study of Psilocybin in Normal Adults

Healthy

United States

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