A Modified Technique to Facilitate Pealing of the Rectal Mucosa in Delorme Operation

Sponsor

Yasser Mohamed Abdel-samii (Other)

Overall Status

Completed

CT.gov ID

NCT02901210

Collaborator

(none)

Enrollment

Arm

Duration (Months)

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate the investigator new modification for delorme procedure in patients with rectal prolapse , assessing intra-operative morbidity and recurrence rate .

Condition or Disease	Intervention/Treatment	Phase
Rectal Prolapse	Procedure: Modified delorme procedure	N/A

Detailed Description

In classic delorme operation stripping of the mucosa done and this is associated with extensive bleeding in addition to the time consumed in this step.the new modification done by the investigator replace this step with another associated with less intraoperative bleeding and not time consuming.

Study Design

Study Type:

Interventional

Actual Enrollment :

25 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Study Start Date :

Jan 1, 2015

Actual Primary Completion Date :

Jan 1, 2016

Actual Study Completion Date :

Aug 1, 2016

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Modified Delorme Modified technique for delorme procedure done in mild to moderate rectal prolapse as the investigator destroy use the electrocautery to peal the mucosa with less intraoperative bleeding ,avoiding stripping of the mucosa done in classic delorme that induce major bleeding intraoperative .	Procedure: Modified delorme procedure

Arm

Intervention/Treatment

Experimental: Modified Delorme

Modified technique for delorme procedure done in mild to moderate rectal prolapse as the investigator destroy use the electrocautery to peal the mucosa with less intraoperative bleeding ,avoiding stripping of the mucosa done in classic delorme that induce major bleeding intraoperative .

Procedure: Modified delorme procedure

Outcome Measures

Primary Outcome Measures

Recurrence rate assessed in this modified technique [One year follow up post operative]
intraoperative bleeding measured in this modified technique [one year follow up post operative.]

Eligibility Criteria

Criteria

Ages Eligible for Study:

N/A and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Mild to moderate rectal prolapse
Singed informed consent.

Exclusion Criteria:

Huge rectal prolapse .
Recurrent rectal prolapse

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

Yasser Mohamed Abdel-samii

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Yasser Mohamed Abdel-samii, Lecturer of general surgery., Ain Shams University

ClinicalTrials.gov Identifier:

NCT02901210

Other Study ID Numbers:

IRB00006379

First Posted:

Sep 15, 2016

Last Update Posted:

Sep 15, 2016

Last Verified:

Sep 1, 2016

Individual Participant Data (IPD) Sharing Statement:

Undecided

Plan to Share IPD:

Undecided

Keywords provided by Yasser Mohamed Abdel-samii, Lecturer of general surgery., Ain Shams University

Recta prolapse

Intraoperative bleeding

mucosal cauterization

Additional relevant MeSH terms:

Rectal Prolapse

Prolapse

Study Results

No Results Posted as of Sep 15, 2016