Last reviewed · How we verify

NCT06559085

Posterior Versus Lateral Laparoscopic Mesh Rectopexy for the Management of Complete Rectal Prolapse

Recruiting now NA Last updated 19 August 2024
What this trial tests

NA trial testing Laproscopic posterior mesh rectopexy (Wells or LPMR) in Posterior Laparoscopic in 30 participants. Currently enrolling.

Timeline
15 August 2024
Primary endpoint
1 October 2026
1 October 2026

Quick facts

Lead sponsorAssiut University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment30
Start date15 August 2024
Primary completion1 October 2026
Estimated completion1 October 2026
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

Adults 18 to 75, any sex, with Posterior Laparoscopic or Lateral Laparoscopic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Aim of the study is to evaluate the outcomes of two different methods of mesh placement during laparoscopic rectopexy for the management of complete rectal prolapse lateral versus posterior mesh rectopexy

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other Assiut 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/NCT06559085.

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