Skip to content

Anterior Versus Posterior Laparoscopic Mesh Rectopexy For Rectal Prolapse; a Randomized Controlled Trial.

Anterior Versus Posterior Laparoscopic Mesh Rectopexy For Rectal Prolapse; a Randomized Controlled Trial.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03026738
Enrollment
30
Registered
2017-01-20
Start date
2017-01-31
Completion date
2019-12-31
Last updated
2017-01-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rectal Prolapse

Brief summary

Aim of this work is to compare results between Laparoscopic Anterior Mesh Rectopexy and Laparoscopic Posterior Mesh Rectopexy for patients with rectal prolapse by assessment of operative time, intraoperative blood loss , intraoperative organ injury, overall length of hospital stay, recurrence,and improvement of incontinence and constipation.

Detailed description

Rectal prolapse is a disabling condition, which is more common in females and increases in frequency with age. There are two types of rectal prolapse; external and internal. External rectal prolapse is a circumferential protrusion of all layers of the rectum through the anal sphincter. Internal rectal prolapse, also referred to as rectal intussusception. The majority of patients with a RP suffer from symptoms of fecal incontinence and constipation, causing a significant negative impact on quality of life. The aims of the surgical treatment are to correct the anatomical abnormality and to cure the accompanying symptoms of incontinence, constipation and pain, with the lowest rate of complications as possible and an acceptable rate of recurrence. Since the emergence of minimally invasive surgery, laparoscopic techniques for the treatment for RP have been applied in patients of all ages.

Interventions

fixation of the rectum anteriorly using laparosopy and polypropylene mesh

PROCEDURELaparoscopic posterior mesh rectopexy

fixation of the rectum posteriorly using laparosopy and polypropylene mesh

A strip of polypropylene mesh will be introduced and sutured.

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* all patients with rectal prolapse either external or internal prolapse

Exclusion criteria

* Age below 18 years. * Pregnancy or breast-feeding. * Recurrence of rectal prolapse. * patients with previous complicated abdominal surgery.

Design outcomes

Primary

MeasureTime frame
improvement of incontinence and / or constipation.1 year postoperatively
recurrence rate1 year postoperatively

Secondary

MeasureTime frameDescription
Duration of SurgeryintraoperativeThe duration of the procedure will be registered in minutes.
Peri-operative blood lossduring surgery, 1 dayBlood loss will be measured in milliliters

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026