Comparative study of the effects of Daikenchuto and lactobacillus preparation on abdominal symptoms after laparoscopic sacrocolpopex for pelvic organ prolapse: A randomized, prospective study

Phase 4

Recruiting

• Conditions: pelvic organ prolapse

• Registration Number: JPRN-UMIN000040129
• Lead Sponsor: Department of urology, Hokusuikai Kinen Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-05-01
• Last Update Posted: 17 October 2023
• Study Completion: 2026-05-31

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Not provided

Exclusion Criteria

Patients with a history of allergy to Daikenchuto and lactobacillus preparation. Patients who have been taking oral medications with Daikenchuto and lactobacillus preparation within the past 6 months. In addition, patients whose physicians deem it inappropriate to participate in this study.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary outcomes included time to first flatus, bowel movement, and tolerance of diet after extubation.

Secondary Outcome Measures

Name	Time	Method
CRAD-8, VAS scale, white blood cell counts, C-reactive protein (CRP) level and length of hospital stay