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NCT03411226: re-TREPP
Feasibility of Re-TREPP in Patients With a Recurrent Inguinal Hernia After Previous TREPP Repair
trial testing re-TREPP in Recurrent Inguinal Hernia in 19 participants. Completed in 31 January 2016.
10 December 2015
Quick facts
| Lead sponsor | Alexandra Persoon |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 19 |
| Start date | 27 November 2015 |
| Primary completion | 10 December 2015 |
| Estimated completion | 31 January 2016 |
Drugs / interventions tested
- re-TREPP
Conditions studied
- Recurrent Inguinal Hernia — all drugs for Recurrent Inguinal Hernia →
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:
- PubMed search for NCT03411226
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Recurrent Inguinal Hernia
Currently open trials in the same condition.
- NCT06604572 — TAPP and Open Repair for Recurrent Inguinal Hernia · NA · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03411226 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Alexandra Persoon
- Last refreshed: 29 January 2018
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