Modified Perineal Linear Stapler Resection for External Rectal Prolapse: a Novel Approach

Sponsor
Zagazig University (Other)
Overall Status
Completed
CT.gov ID
NCT04184310
Collaborator
(none)
36
1
1
30
1.2

Study Details

Study Description

Brief Summary

from December 2016 to July 2019, 36 elderly co-morbid patients with rectal prolapse were involved in this study which is performed in the GIT surgery unit of Zagazig University Hospital. the investigators used a modified linear stapler resection technique for the rectal prolapse. Postoperative follow up was done for one year to evaluate functional outcome, operative time, hospital stay and complications

Condition or Disease Intervention/Treatment Phase
  • Other: Modified perineal linear stapler resection for external rectal prolapse
N/A

Detailed Description

The study was done in the GIT Unit of the General Surgery Department of Zagazig University Hospital in the period from December 2016 to July 2019. The hospital Institutional Review Board approved the study protocol. Thirty-six old, co-morbid and short life expectancy patients were included in the sample. They were evaluated for PSP. Informed consent was signed by all patients or first-degree relatives after full discussion of the advantage and disadvantage of the operation. Preoperative bimanual examination was done for rectal prolapse to rule out enterocele or cystocele and this was confirmed by MRI. The routine preoperative evaluation was done for all patients (physical examination, complete blood tests, ECG and chest x-ray). Bowel preparation was done for all patients.

Regarding bowel function, all patients were evaluated for fecal incontinence by Wexner score and for constipation by Rome II criteria. Prophylactic intravenous cephalosporin and metronidazole was given one hour before operation. The operation was done under spinal anesthesia in the lithotomy position with slight Trendeleburg to prevent trapping of abdominal organs between walls of rectum. All operations were done by the same surgical members of the unit. Hospital stay, Intraoperative and postoperative complications were recorded. All patients started oral fluids in the second day. Follow up was done for patients every 1,3,6,9 and 12 months in the outpatient clinic.

Study Design

Study Type:
Interventional
Actual Enrollment :
36 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Modified Perineal Linear Stapler Resection for External Rectal Prolapse: a Novel Approach
Actual Study Start Date :
Dec 5, 2016
Actual Primary Completion Date :
Jul 5, 2018
Actual Study Completion Date :
Jun 5, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: old patient with rectal prolapse

old co-morbid patient with complete rectal prolapse unfit for abdominal operation

Other: Modified perineal linear stapler resection for external rectal prolapse
After anesthesia and patient position, the prolapse was pulled out Two vertical incision were made in both the inner and outer walls of the prolapse (at 3and 9 o'clock)1-2 cm in size approximately 2 cm above the dentate line. We used a reloadable linear cutter stapler (GIA 100mm Covidien, Mansfield, Mass., USA) passing through the tunnel to cut the anterior aspect of the prolapse . Then, after reload the stapler by the new cartridge, we used it to do the same for posterior wall and the prolapsed rectum was completely transected . We ensure that the stapler did not fire at the dentate line to avoid post-operative pain. Multiple 3-0 PDS intermittent full thickness sutures were done for hemostasis. The prolapsed rectum falls back into place spontaneously.

Outcome Measures

Primary Outcome Measures

  1. treatment of rectal prolapse [30 dyas]

    patients satisfaction after operation - no mass coming form anus - no previous complications like bleeding and constipation

Secondary Outcome Measures

  1. post operative complications [one year]

    bleeding - infection - constipation-incontinence- recurrence

Eligibility Criteria

Criteria

Ages Eligible for Study:
48 Years to 95 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • old age

  • complete rectal prolapse

  • co-morbid ASA I to III

Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Zagazig Unversity Zagazig Egypt

Sponsors and Collaborators

  • Zagazig University

Investigators

  • Principal Investigator: osama khalil, Ph.d, assistant professor

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
osama khalil, assistant profeosser, Zagazig University
ClinicalTrials.gov Identifier:
NCT04184310
Other Study ID Numbers:
  • IR-170133-1
First Posted:
Dec 3, 2019
Last Update Posted:
Dec 3, 2019
Last Verified:
Nov 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 3, 2019