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NCT04839848
Chronic Postoperative Pain After the Lichtenstein Groin Hernioplasty
trial testing Lichtenstein mesh repair in Hernia, Inguinal in 80,733 participants. Completed in 6 November 2020.
6 November 2019
Quick facts
| Lead sponsor | Karolinska Institutet |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 80,733 |
| Start date | 1 September 2012 |
| Primary completion | 6 November 2019 |
| Estimated completion | 6 November 2020 |
Drugs / interventions tested
- Lichtenstein mesh repair
Conditions studied
- Hernia, Inguinal — all drugs for Hernia, Inguinal →
- Hernia, Femoral — all drugs for Hernia, Femoral →
- Postoperative Pain — all drugs for Postoperative Pain →
- Chronic Pain — all drugs for Chronic Pain →
Sponsor
Karolinska Institutet
Who can join
15 and older, any sex, with Hernia, Inguinal or Hernia, Femoral. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The study attempts to quantify the relative risks for chronic postoperative inguinal pain (CPIP) after Lichtenstein repair of groin hernia, depending on mesh type and fixation suture material. For this purpose the investigators will analyze data from the Swedish Hernia Registry (SHR).
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 NCT04839848
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Hernia, Inguinal
Currently open trials in the same condition.
- NCT05934266 — Impact of Mesh Fixation With Tissue Adhesive · Phase 4 · active not recruiting
- NCT05839587 — Transabdominal Preperitoneal Inguinal Hernia Repair · NA · active not recruiting
- NCT05484635 — Mesh Removal Versus No Mesh Removal for Chronic Groin Pain After Inguinal Hernia Repair · NA · recruiting
- NCT05216276 — Robotic vs. Conventional Minimal-invasive Inguinal Hernia Repair · NA · active not recruiting
- NCT04779918 — Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh · NA · recruiting
Other Karolinska Institutet trials
Trials by the same sponsor.
- NCT06359262 — Evaluating the Hope@School Prevention Program · NA · not yet recruiting
- NCT07289490 — Bilateral vs Unilateral Inguinal Hernia Repairs With an Asymptomatic Inguinal Hernia in Bilateral Hernias · NA · not yet recruiting
- NCT06894264 — Emotion Processing and Regulation in People With Intellectual Disability · NA · not yet recruiting
- NCT07494266 — Safety of a Healthy Plant-based Diet With Higher Potassium Content, Compared to a Healthy Plant-based Diet With Limited · NA · not yet recruiting
- NCT07442032 — Cardiovascular Phenotypes in Sepsis · not yet 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 NCT04839848 (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 Karolinska Institutet
- Last refreshed: 5 December 2022
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/NCT04839848.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing