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A preliminary study to explore clinical endpoints in patients (male) with diarrhea-predominant irritable bowel syndrome

This trial is complete
The study has ended normally, and participants are no longer being examined or treated (that is, the last participant's last visit has occurred).

Clinicaltrials.gov ID

The unique identification code given to each clinical study upon registration at ClinicalTrials.gov.
NCT00918411

Astellas Study ID

The unique identification code given by the study sponsor.

060-CL-500

EudraCT ID

The unique identification code given to each clinical study upon registration at EudraCT (European Union Drug Regulating Authorities Clinical Trials Database).

N/A

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Condition

Irritable Bowel Syndrome (IBS)

Phase

These clinical trials happen after a drug or treatment has been approved for patients to take. Clinical trials in phase 4 usually take place over many years because researchers want to learn about long term use and safety of a drug or treatment.

Phase 4

Age

20 Years - 64 Years

Sex

Male

Product

N/A

Type

A type of clinical study in which participants are assigned to groups that receive one or more intervention/treatment (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.

Interventional

Trial Dates

Jun 2009 - Dec 2009

Masking

Single (Participant)

Enrollment number

98

Post-marketing clinical study of ramosetron hydrochloride (Irribow Tablets) - A preliminary study to evaluate the co-primary endpoint in patients (male) with diarrhea-predominant irritable bowel syndrome

Study summary

Study documents

Study Documents, including study results, are available after a study is completed or terminated, according to Astellas Transparency policy.

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