Prophylactic Use of ciNPWT in Gynecologic Laparotomy
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity Hospital Hradec Kralove
About this trial
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
Eligibility criteria
Qualifiers
Adult female patients scheduled for planned abdominal surgery for gynecologic or gynecologic-oncologic indications.
Disqualifiers
Failure to provide informed consent.
Trial design
Treatments tested in this trial
- closed incision negative pressure wound therapy (ciNPWT)
Treatment groups
30 Participants
are divided into 2 treatment groupsLocations
Sponsors and collaborators
Source ClinicalTrials.gov