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A multicenter prospective study to evaluate the effect of elobixibat on spontaneous defecation without a feeling of residual stool in patients with chronic constipation who are inadequately effective with magnesium oxide, a first-line treatment for constipation.

Not Applicable
Recruiting
Conditions
chronic constipation
Registration Number
JPRN-UMIN000048397
Lead Sponsor
Medical corporation Irisawa Medical Clinic
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
26
Inclusion Criteria

Not provided

Exclusion Criteria

1) Patients with a history of hypersensitivity to elobixibat 2) Patients with confirmed or suspected intestinal obstruction due to tumor, hernia, etc. 3) Patients suspected of having constipation due to organic disease 4) Patients taking other laxatives 5) Others who are judged by the principal investigator to be inappropriate as research subjects

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Difference in spontaneous bowel movements (SBM) before and after switching to study drug
Secondary Outcome Measures
NameTimeMethod
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