Pexy Versus Non-pexy for Full Thickness Rectal Prolapse (Bergamaschi)
Primary Purpose
Rectal Prolapse
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
sacral rectopexy with sutures or meshes
full rectal mobilization from the sacrum without sacral rectopexy
Sponsored by
About this trial
This is an interventional treatment trial for Rectal Prolapse focused on measuring Rectal prolapse, mesh, recurrence
Eligibility Criteria
Inclusion Criteria:
- informed consent
- mental ability to understand the procedure
- age range 18 to 70
- both sex
Exclusion Criteria:
- patients with recurrent rectal prolapse
- previous pelvic or colorectal surgery
- previous operation for fecal incontinence
- Cancer
- chronic intestinal Inflammatory diseases
Sites / Locations
- Stony brook University
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Sham Comparator
Arm Label
Pexy group
Non-pexy group
Arm Description
This group of patients with full thickness rectal prolapse will receive standard sacral rectopexy with mesh or sutures
These patients will receive full rectal mobilization from the sacrum but without rectopexy
Outcomes
Primary Outcome Measures
long term recurrence of the rectal prolapse
Secondary Outcome Measures
Full Information
NCT ID
NCT01022034
First Posted
November 25, 2009
Last Updated
December 1, 2009
Sponsor
Societa Italiana di Chirurgia ColoRettale
1. Study Identification
Unique Protocol Identification Number
NCT01022034
Brief Title
Pexy Versus Non-pexy for Full Thickness Rectal Prolapse
Acronym
Bergamaschi
Official Title
Pexy vs. No Pexy in Abdominal Surgery for Full Thickness Rectal Prolapse in Adults: A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
December 2009
Overall Recruitment Status
Completed
Study Start Date
January 2003 (undefined)
Primary Completion Date
January 2009 (Actual)
Study Completion Date
October 2009 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Societa Italiana di Chirurgia ColoRettale
4. Oversight
5. Study Description
Brief Summary
No randomized controlled trial (RCT) has compared no rectopexy to rectopexy for external full-thickness rectal prolapse (FTRP). This study was performed to test the hypothesis that recurrence rates for FTRP following no rectopexy are not inferior to those for rectopexy.
Method: This is a multicenter randomized non-inferiority trial. Eligible patients were randomized to no rectopexy or rectopexy. The no rectopexy arm was defined as abdominal surgery with rectal mobilization only. The rectopexy arm was defined as abdominal surgery with mobilization and pexy. Sigmoid resection was not randomized and was added in the presence of constipation. The endpoint was recurrence rates defined as presence of external FTRP after surgery. A pre-RCT meta-analysis suggested a sample size of 251 patients based on a 15% expected difference in the 5-year cumulative recurrence rate. Recurrence-free curves will be generated and compared using the Kaplan-Meier method and log-rank test, respectively. A Bonferroni adjustment was used. An adjusted p value of <0.01 was considered significant.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Prolapse
Keywords
Rectal prolapse, mesh, recurrence
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
180 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Pexy group
Arm Type
Active Comparator
Arm Description
This group of patients with full thickness rectal prolapse will receive standard sacral rectopexy with mesh or sutures
Arm Title
Non-pexy group
Arm Type
Sham Comparator
Arm Description
These patients will receive full rectal mobilization from the sacrum but without rectopexy
Intervention Type
Procedure
Intervention Name(s)
sacral rectopexy with sutures or meshes
Intervention Type
Procedure
Intervention Name(s)
full rectal mobilization from the sacrum without sacral rectopexy
Primary Outcome Measure Information:
Title
long term recurrence of the rectal prolapse
Time Frame
after 5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
informed consent
mental ability to understand the procedure
age range 18 to 70
both sex
Exclusion Criteria:
patients with recurrent rectal prolapse
previous pelvic or colorectal surgery
previous operation for fecal incontinence
Cancer
chronic intestinal Inflammatory diseases
Facility Information:
Facility Name
Stony brook University
City
New York
State/Province
New York
ZIP/Postal Code
11794-3368
Country
United States
12. IPD Sharing Statement
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Pexy Versus Non-pexy for Full Thickness Rectal Prolapse
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