Status:
COMPLETED
Chronic Postoperative Pain After the Lichtenstein Groin Hernioplasty
Lead Sponsor:
Karolinska Institutet
Collaborating Sponsors:
Uppsala University
Swedish Hernia Registry
Conditions:
Hernia, Inguinal
Hernia, Femoral
Eligibility:
All Genders
15+ years
Brief Summary
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 th...
Detailed Description
This is an open cohort study design where the investigators will analyze existing data that have been prospectively collected in SHR, which covers \> 95% of all groin hernia repairs in Sweden. The lar...
Eligibility Criteria
Inclusion
- All Lichtenstein and similar open mesh repairs that have been registered in the SHR from September 1, 2012, until December 31, 2018.
Exclusion
- Laparoscopic repairs.
- Preperitoneal open repairs.
- Pure suture repairs
- Patients not having a 10-digit state-assigned Patient Identification Number.
Key Trial Info
Start Date :
September 1 2012
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
November 6 2020
Estimated Enrollment :
80733 Patients enrolled
Trial Details
Trial ID
NCT04839848
Start Date
September 1 2012
End Date
November 6 2020
Last Update
December 5 2022
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