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Opioid-Induced Bowel Dysfunction clinical trials

View clinical trials related to Opioid-Induced Bowel Dysfunction.

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NCT ID: NCT06385561 Completed - Constipation Clinical Trials

The Influence of Tramadol on Opioid-induced Bowel Dysfunction

Start date: August 11, 2022
Phase: Phase 2
Study type: Interventional

Tramadol is a weak opioid and widely used to treat moderate to severe pain. Stronger opioids are known to inhibit gastrointestinal motility and secretion, however the effects of tramadol on gastrointestinal function remains less understood. The aim of this study was to determine to what degree tramadol causes opioid-induced bowel dysfunction by using an objective design to explore gastrointestinal transit, motility pattern, secretion, and colonic volume, in a group of healthy male volunteers.

NCT ID: NCT01298219 Completed - Clinical trials for Opioid-induced Bowel Dysfunction

Opioid-induced Bowel Dysfunction (OBD) Pivotal Assessment of Lubiprostone (OPAL)

Start date: December 2010
Phase: Phase 3
Study type: Interventional

The primary purpose of the study is to evaluate the efficacy and safety of lubiprostone administration in subjects with Opioid-induced Bowel Dysfunction.

NCT ID: NCT01122030 Completed - Clinical trials for Opioid Induced Bowel Dysfunction

Study to Evaluate the Safety and Efficacy of S-297995 for the Treatment of Opioid-Induced Bowel Dysfunction in Subjects With Chronic Pain

Start date: April 2010
Phase: Phase 2
Study type: Interventional

Study consists of 6 treatment cohorts of 12 subjects with chronic pain, opioid-induced bowel dysfunction, and opioid physical dependence. Total duration of treatment for each subject will be up to 28 days. Each subject will receive a single dose of study drug, administered orally in the morning of Day 15 under fasted conditions. Cohort 1: 0.1 mg of S-297995 or placebo. Cohort 2: 0.3 mg of S-297995 or placebo. Cohort 3: 1 mg of S-297995 or placebo. Cohort 4: 3 mg of S-297995 or placebo. Cohort 5: 0.03 mg of S-297995 or placebo. Cohort 6: 0.01 mg of S-297995 or placebo. The primary objective of the study is to evaluate the safety of single doses of oral S-297995 in subjects physically dependent on opioids

NCT ID: NCT00620061 Completed - Clinical trials for Opioid-Induced Bowel Dysfunction

Opioid-induced Bowel Dysfunction: Long-Term Assessment of Lubiprostone

Start date: December 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the long-term safety and efficacy of lubiprostone administration in participants with opioid-induced bowel dysfunction.

NCT ID: NCT00597428 Completed - Clinical trials for Opioid-Induced Bowel Dysfunction

Opioid-induced Bowel Dysfunction Pivotal Assessment of Lubiprostone

OPAL
Start date: August 2007
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to evaluate the efficacy and safety of lubiprostone administration in patients with opioid-induced bowel dysfunction (OBD).

NCT ID: NCT00595946 Completed - Clinical trials for Opioid-Induced Bowel Dysfunction

Opioid-induced Bowel Dysfunction: Pivotal Assessment of Lubiprostone

OPAL
Start date: August 2007
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to evaluate the efficacy and safety of lubiprostone administration in patients with Opioid-induced Bowel Dysfunction.