Randomised Trial of Rectal Prolapse Surgery

Completed

• Conditions: Full thickness rectal prolapse; Urological and Genital Diseases

• Registration Number: ISRCTN01911755
• Lead Sponsor: Clinical Trials Unit University of Birmingham (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2003-11-20
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 1000

Inclusion Criteria

Patients eligible for this study will be those with full thickness rectal prolapse.

Exclusion Criteria

Not provided at time of registration

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary measures of efficacy will be recurrence of rectal prolapse for randomisation 1 and bowel function for randomisation 2.

Secondary Outcome Measures

Name	Time	Method
ot provided at time of registration