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Efficacy and Safety of Prunus Mume Extract on Improvement of Constipation

Constipation Clinical Trial

Clinical Trial Summary

The investigators performed a 8-week, randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of Prunus Mume Extract on Improvement of Constipation. The investigators measured Improvement of Constipation parameters , including Colonic Transit Time, number of bowel movement, defecation time, stool type, color and stool amounts per defecation, and monitored their blood pressure.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01734226
Study type Interventional
Source Chonbuk National University Hospital
Contact
Status Recruiting
Phase Phase 2/Phase 3
Start date August 2012
Completion date December 2012
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