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Prevention of Postoperative Hernias in Emergency Surgery

Study acronym: PROPHECY
StatusRecruiting
PhaseNot specified
Started
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Record History

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  1. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    v5
  2. Primary completion date: Dec 31, 2025 to Dec 31, 2026
    • Enrollment target: 375 to 500
    • Study description expanded, about 3 words
    v4
  3. Enrollment target: 400 to 375
    • Eligibility criteria shortened, about 7 words
    • Study description expanded, about 642 words
    • Publications: 5 to 11
    v3
  4. Start date: Apr 1, 2025 to Jun 1, 2025
    • Primary completion date: Oct 31, 2025 to Dec 31, 2025
    • Study completion date: Oct 31, 2026 to Dec 31, 2026
    v2
  5. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 aim of this observational study is to understand the risk factors and incidence of postoperative hernias among patients undergoing emergency surgery. The main question it aims to answer is: What is the incidence of postoperative hernias in this group of patients? A brief telephone interview will be conducted with participants who will be included in this study one year after the surgery. If the presence of a postoperative hernia is suspected, the patient will be invited to a follow-up visit to the surgical clinic, where the diagnosis will be confirmed by imaging tests.
Trial Details
NCT Number NCT06815822
Lead Sponsor Jan Kochanowski University
Conditions
(from sponsor)		 Incarcerated Hernia, Appendicitis Acute, Cholecystitis, Acute, Ileus, Perforated Gastro-duodenal Ulcers, Perforated Bowel
Related terms Appendicitis, Cholecystitis, Acute, Ileus, Incisional Hernia, Intestinal Perforation
Enrollment 500 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov