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NCT04334421

APEMESH- Preventing Perineal Complications After Abdominoperineal Resection

Completed Last updated 1 February 2024
What this trial tests

trial testing Composite mesh in Rectal Cancer in 30 participants. Completed in 28 February 2022.

Timeline
3 April 2020
Primary endpoint
28 February 2021
28 February 2022

Quick facts

Lead sponsorElisa Mäkäräinen
StatusCompleted
Study typeOBSERVATIONAL
Enrollment30
Start date3 April 2020
Primary completion28 February 2021
Estimated completion28 February 2022
Sites1 location across Finland

Drugs / interventions tested

Conditions studied

Sponsor

Elisa Mäkäräinen

Who can join

18 and older, any sex, with Rectal Cancer or Abdominoperineal Resection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Abdominoperineal resection leaves an empty space to be filled by mesh or musculocutaneus flap. Several studies have reported over 30% morbidity with perineal wound healing after abdominoperineal resection. Preoperative radiotherapy is a strong predictor for perineal complications. Musculocutaneus flaps and use of biological mesh seem to minimize perineal morbidity. The role of omentoplasty at APR is controversial. Previous studies on synthetic mesh repair on perineum are almost lacking.

Publications & conference data

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

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Other recruiting trials for Rectal Cancer

Currently open trials in the same condition.

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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/NCT04334421.

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