Prophylactic Use of ciNPWT in Gynecologic Laparotomy

Starting soon · Not applicable

Conditions studied: Surgical Site Infection (SSI), Wound Healing Complication, Seroma, Hematoma, Dehiscence

In brief

This is a prospective, open-label, non-randomized interventional feasibility study with a nested qualitative analysis. The study exploratively verifies the feasibility of targeted prophylactic closed incision negative pressure wound therapy (ciNPWT) in clinical practice for patients with a high predicted risk of wound healing complications and compares the 30-day incidence of postoperative complications with standard dressing. Participants will: * Get ciNPWT or standard dressing after planned laparotomy * Answer the questionairs about qualite of life * Will visit the clinic 30 days after surgery to see the final result

Key facts

Study ID

NCT07645547

Run by

University Hospital Hradec Kralove

People needed

30

Starts

2026-07-01

Expected to finish

2028-12-01

Last updated by the study team

2026-06-12

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Adult female patients scheduled for planned abdominal surgery for gynecologic or gynecologic-oncologic indications.
• Identification as "high-risk" for wound healing complications based on a clinical risk screening at admission.
• Signed informed consent.

You may not qualify if…

• Failure to provide informed consent.

Full record on ClinicalTrials.gov

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