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CompletedNCT02901210Updated Sep 15, 2016

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

An interventional study of Modified delorme procedure in Rectal Prolapse, sponsored by Yasser Mohamed Abdel-samii. Completed. Per ClinicalTrials.gov, last updated 2016-09-15.

Sponsored by Yasser Mohamed Abdel-samii · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
25
Allocation
Not applicable
Sex
All
01

Study 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 .

Read the 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.

02

Conditions studied

  • Rectal Prolapse

Keywords

  • Recta prolapse
  • Intraoperative bleeding
  • mucosal cauterization
03

In context

Rectal Prolapse

55 studies on the registry are indexed under Rectal Prolapse; 12 are open to participants now.

This study's enrollment of 25 is below the median of 55 across 34 interventional studies indexed under Rectal Prolapse.

Browse Rectal Prolapse studies →

Lead sponsor

Yasser Mohamed Abdel-samii is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Mild to moderate rectal prolapse
  • Singed .

Exclusion criteria

Exclusion Criteria:

  • Huge rectal prolapse .
  • Recurrent rectal prolapse
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
25 participants (actual)

Study arms

  • 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

Interventions

  • ProcedureModified delorme procedure
06

What researchers measure

Primary outcomes

  1. Recurrence rate assessed in this modified technique

    Time frame: One year follow up post operative

  2. intraoperative bleeding measured in this modified technique

    Time frame: one year follow up post operative.

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 15, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02901210
Lead sponsor
Yasser Mohamed Abdel-samii
Responsible party
Yasser Mohamed Abdel-samii (Lecturer of general surgery., Ain Shams University) — Sponsor-investigator
First posted
Sep 15, 2016
Start date
Jan 2015
Primary completion
Jan 2016
Completion
Aug 2016
Last update
Sep 15, 2016

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.

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Discussion

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