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Prophylactic Use of ciNPWT in Gynecologic Laparotomy

NCT07645547 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-06-12

No results posted yet for this study

Summary

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

Conditions

  • Surgical Site Infection (SSI)
  • Wound Healing Complication
  • Seroma
  • Hematoma
  • Dehiscence

Interventions

DEVICE

closed incision negative pressure wound therapy (ciNPWT)

targeted prophylactic closed incision negative pressure wound therapy in clinical practice for patients with a high predicted risk of wound healing complications

Sponsors & Collaborators

  • University Hospital Hradec Kralove

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-07-31
Primary Completion
2028-06-30
Completion
2028-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07645547 on ClinicalTrials.gov