Status:
UNKNOWN
Suture Techniques to Reduce the Incidence of Incisional Hernia: LTFU STITCH Trial
Lead Sponsor:
Erasmus Medical Center
Collaborating Sponsors:
Franciscus &Vlietland
Elisabeth-TweeSteden Ziekenhuis
Conditions:
Surgery
Incisional Hernia
Eligibility:
All Genders
18-110 years
Phase:
NA
Brief Summary
Rationale: Incisional hernias (IH) are a frequent complication after abdominal surgery. Prevalence of an IH varies depending on the previous abdominal procedure but could be as high as 70% in high-ris...
Detailed Description
Rationale: Incisional hernias (IH) are a frequent complication after abdominal surgery. Prevalence of an IH varies depending on the previous abdominal procedure but could be as high as 70% in high-ris...
Eligibility Criteria
Inclusion
- In order to be eligible to participate in this study, a subject must meet the following criteria:
- Available signed informed consent form for the original STITCH trial of the patients who are still alive.
- Or if the patients has died, the medical records are reviewed.
- A potential subject who meets the following criteria will be excluded from participation in this study:
- \- Patients that on the original informed consent form of the STITCH trial, checked the box that they did not want to be approached for future follow-up studies.
Exclusion
Key Trial Info
Start Date :
August 1 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
October 1 2024
Estimated Enrollment :
560 Patients enrolled
Trial Details
Trial ID
NCT06066385
Start Date
August 1 2023
End Date
October 1 2024
Last Update
October 4 2023
Active Locations (9)
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1
Erasmus MC
Rotterdam, South Holland, Netherlands, 3015
2
Meander Medical Center
Amersfoort, Netherlands
3
Rijnstate ziekenhuis
Arnhem, Netherlands
4
Red Cross Hospital
Beverwijk, Netherlands