Clinical trial · Interventional
Prophylactic Use of ciNPWT in Gynecologic Laparotomy
Implementation of Prophylactic Negative Pressure Wound Therapy (ciNPWT) in High-Risk Patients in Gynecologic Oncology: A Prospective Feasibility Study and Nested Qualitative Analysis
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Dehiscence | — | UNRESOLVED | — |
| Hematoma | — | UNRESOLVED | — |
| Seroma | — | UNRESOLVED | — |
| Surgical Site Infection (SSI) | — | UNRESOLVED | — |
| Wound Healing Complication | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| closed incision negative pressure wound therapy (ciNPWT) | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Preventive ciNPWT
- interventionNames
- Device: closed incision negative pressure wound therapy (ciNPWT)
- type
- NO_INTERVENTION
- label
- Standard dressing
Primary outcomes (3)
- measure
- Feasibility of targeted prophylactic ciNPWT
- timeFrame
- Up to 30 postoperative days
- description
- Feasibility of prophylactic ciNPWT described as: Recruitment rate (%)
- measure
- Feasibility of targeted prophylactic ciNPWT
- timeFrame
- Up to 30 postoperative days
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * 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. Exclusion Criteria: * Failure to provide informed consent.
References
Publications (0)
Data not yet available