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NCT05894226

Functional and Sexual Outcomes After Laparoscopic Ventral Mesh Rectopexy for Complex Rectocele

Completed NA Last updated 8 June 2023
What this trial tests

NA trial testing laparoscopic ventral mesh rectopexy in Rectocele in 15 participants. Completed in 30 August 2022.

Timeline
1 March 2021
Primary endpoint
1 February 2022
30 August 2022

Quick facts

Lead sponsorMansoura University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment15
Start date1 March 2021
Primary completion1 February 2022
Estimated completion30 August 2022
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Mansoura University

Who can join

Adults 30 to 60, female only, with Rectocele or Obstructive Defecation Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The ideal surgical strategy for treating complex rectocele remains a topic for debate, with the transanal, transperineal, and transvaginal approach and the abdominal approach being at conflict with one another. While the transvaginal repair is more popular among gynecologists, the trans abdominal approach has become increasingly common among colorectal surgeons, in part due to the rising demand for minimally invasive surgery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of laparoscopic ventral mesh rectopexy

Trials testing the same drug.

Other recruiting trials for Rectocele

Currently open trials in the same condition.

Other Mansoura University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05894226.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing