Clinical trial Recruiting at 1 site Interventional

Transverse versus longitudinal groin incision for vascular surgery

Official title: The Incidence of Surgical Site Complications in Transverse Versus Longitudinal Groin Incision in Vascular Surgery: A Randomized Clinical Trial

Run by Kolding Sygehus · NCT06631378 · Data updated 2026-11-12

This compares transverse and longitudinal groin incisions to see if transverse incisions lead to fewer wound problems for people having vascular surgery on the groin.

Quick facts

Study typeInterventional
SexAll
Enrollment232 (estimated)
SponsorKolding Sygehus
Academic / other
Locations1 site (Kolding)
StatusRecruiting
StartedMarch 1, 2025
Main results expectedJune 1, 2027
Study endsJuly 1, 2027
Registry record updatedJune 27, 2025
Trial IDNCT06631378 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults scheduled for elective vascular reconstruction that requires a groin incision and who have not had prior groin surgery and are not undergoing emergency or trauma operations.

Probably not a fit

Patients with previous groin operations, emergency trauma/bleeding or pseudoaneurysm cases, operations within 24 hours of admission, or those needing a planned muscleplasty are excluded and unlikely to benefit from the trial intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized interventional trial assigns patients undergoing vascular reconstruction with a groin incision to either a transverse or a longitudinal incision. Surgeons perform the assigned incision during the planned groin operation and patients are followed for surgical site complications, readmissions, reoperations, length of hospital stay, and amputation rate. Key exclusions include prior groin surgery, emergency operations for trauma/bleeding or pseudoaneurysm, operations within 24 hours of admission, and cases where muscleplasty is planned. Outcomes will be compared between the two incision groups to determine whether incision orientation affects postoperative complications and resource use.

Why it matters

Potential benefit: If successful, the transverse incision approach could reduce groin wound complications, lower readmissions and reoperations, shorten hospital stays, and reduce amputations after groin vascular surgery.

How similar studies have gone: Previous evidence is limited and largely observational with mixed results, so randomized data on whether transverse incisions reduce groin wound complications are scarce.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

• Patients undergoing vascular reconstruction with a groin incision

Exclusion Criteria:

* Patients previously operated with a groin incision.
* Patients undergoing operation due to trauma, bleeding, or pseudoaneurysm.
* Patients operated within the first 24 hours of admission.
* If it prior to the operation is deemed necessary with a muscleplasty.

Where it's running

  • Department of Vascular Surgery - Lillebaelt Hospital
    Kolding, Denmark
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.