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Optimizing Closed Incision Negative Pressure Wound Therapy in Emergency Laparotomy

NCT05716490 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 114

Last updated 2023-11-13

No results posted yet for this study

Summary

The purpose of this study is to find differences in rates of surgical site infections following emergency laparotomy with the use of two different incisional negative pressure wound therapy (iNPWT)devices.

Conditions

  • Surgical Site Infection
  • Surgical Wound
  • Surgical Wound Infection
  • Surgical Complication
  • Surgical Wound Dehiscence
  • Surgical Wound Haemorrhage
  • Surgical Wound, Healed

Interventions

DEVICE

Incisional negative pressure wound therapy

Application of negative pressure wound therapy for prophylaxis of surgical site occurrences

OTHER

Control group - standard wound dressing

Covering of surgical wound with standard wound dressing

Sponsors & Collaborators

  • Centro Hospitalar do Tâmega e Sousa

    lead OTHER

Principal Investigators

  • Marcelo J Costa, MD · Centro Hospitalar do Tâmega e Sousa

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-07-01
Primary Completion
2023-08-01
Completion
2023-09-01

Countries

  • Portugal

Study Locations

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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 NCT05716490 on ClinicalTrials.gov