Last reviewed · How we verify

NCT03411226: re-TREPP

Feasibility of Re-TREPP in Patients With a Recurrent Inguinal Hernia After Previous TREPP Repair

Completed Last updated 29 January 2018
What this trial tests

trial testing re-TREPP in Recurrent Inguinal Hernia in 19 participants. Completed in 31 January 2016.

Timeline
27 November 2015
Primary endpoint
10 December 2015
31 January 2016

Quick facts

Lead sponsorAlexandra Persoon
StatusCompleted
Study typeOBSERVATIONAL
Enrollment19
Start date27 November 2015
Primary completion10 December 2015
Estimated completion31 January 2016

Drugs / interventions tested

Conditions studied

Sponsor

Alexandra Persoon

Who can join

18 and older, any sex, with Recurrent Inguinal Hernia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The Trans REctussheath PrePeritoneal (TREPP) mesh repair was introduced in 2006 to decrease the risk of postoperative inguinal pain in hernia surgery. For the repair of a recurrent inguinal hernia after a primary TREPP an alternative open anterior route (Lichtenstein) may seem the most logical option, but coincides with an increased risk of chronic postoperative inguinal pain. Therefore, this study aimed to evaluate the feasibility of a second TREPP procedure to repair a recurrent inguinal hernia after an initial TREPP repair. The hypothesis was that the technique is possible and does not lead to an increased risk of postoperative pain.

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 recruiting trials for Recurrent Inguinal Hernia

Currently open trials in the same condition.

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/NCT03411226.

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