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Treating Emergency Laparotomy Incisions With Negative Pressure Wound Therapy

Study acronym: TELIN
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

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  1. Secondary endpoints: details revised at 11 of 19 entries
    • Study description revised
    • Site details revised at 4 of 6 sites
    v4
  2. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Sep 2025 to Dec 16, 2025
    • Site details revised at 6 of 6 sites
    v3
  3. Secondary endpoints: details revised at 2 of 19 entriesv2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this clinical trial is to investigate Negative Pressure Wound Therapy (NPWT) in adults undergoing emergency laparotomy. The main question it aims to answer is: Does NPWT decrease wound complications? Researchers will compare it against regular dressings to see if NPWT is superior.
Trial Details
NCT Number NCT07003906
Lead Sponsor Uppsala University
Collaborators: Uppsala County Council, Sweden, Dalarna County Council, Sweden, Sormland County Council, Sweden, Ostergotland County Council, Sweden, Västmanland County Council, Sweden, Landstingens Ömsesidiga Försäkringsbolag (Löf)
Conditions
(from sponsor)		 Surgical Incision, Wound Dehiscence, Surgical Site Infection, Incisional Hernia, Quality of Life
Related terms Incisional Hernia, Surgical Wound, Surgical Wound Infection
Enrollment 720 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov