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Efficacy of ramosetron hydrochloride in male patients with diarrhea-predominant irritable bowel syndrome

Efficacy of ramosetron hydrochloride in male patients with diarrhea-predominant irritable bowel syndrome - Efficacy of ramosetron hydrochloride in male patients with diarrhea-predominant irritable bowel syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000006663
Enrollment
200
Registered
2011-11-10
Start date
2011-11-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diarrhea-predominant irritable bowel syndrome

Interventions

1st step Administration of ramosetron hydrochloride 5 microgram once a day for 4 weeks. 2nd step : increase Administration of ramosetron hydrochloride 10 microgram once a day for 8 weeks. 2nd ste

Sponsors

Shimane University Faculty of Medicine, Department of Gastroenterology and Hepatology
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1) At least 1 question with grade 4 or higher scores in questions 11, 12, and 14. 2) Subjects with written informed consent

Exclusion criteria

Exclusion criteria: 1) Patients who have bowel move disturbance by organic lesion such as IBD (UC and Crohn disease etc.) and cancer. 2) Patients suspected of obstruction in stomach and intestines, and with a history of total gastric resection or bowel resection but not appendectomy 3) Patients with serious complications (liver, kidney, heart, lung, circulatory, or metabolic disorder) 4) Patients with a history of drug allergy 5) Others, including patients who are unfit for the study as determined by the attending doctor 6) Patients who are taking polycarbophil calcium.

Design outcomes

Primary

MeasureTime frame
Efficacy of ramosetron hydrochloride in patients with diarrhea-predominant irritable bowel syndrome (Indicator: GSRS).

Secondary

MeasureTime frame
Reliability and validity of the Izumo scale in the monitoring of symptoms in patients with irritable bowel syndrome

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026