Optimization of Surgical Treatment of Patients With Incisional Ventral Hernias

StatusCompleted
PhaseNot applicable
Started

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Record History

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  1. Minor Trial completed Show 4 more changesShow less
    • Study description expanded, about 22 words
    • Site details revised
    • Publications: details revised at 10 of 10 entries
    • Eligibility criteria expanded, about 2 words
  2. Notable Primary completion date: Apr 30, 2024 to Apr 30, 2025
    • Primary endpoints: 2 to 3
    • Secondary endpoints: 1 to 2
    • Study description shortened, about 73 words
    v2
  3. Study First Submitted
  • 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 our work of optimization of the treatment of postoperative hernias is to improve the results of treatment of patients with median and median-lateral postoperative hernias of medium (W2) and large (W3) sizes by developing new surgical techniques. The main questions it aims to answer are: 1. To study the topographic and variant anatomy of vessels and nerves in the retromuscular, preperitoneal, postperitoneal and pre-abdominal cell spaces of the anterior abdominal wall. To determine the most probable sources of blood flow and lymph from the anatomical formations forming the bed of the endoprosthesis. 2. To develop technical, surgical techniques that allow to form an implant bed with minimal traumatization of blood vessels and nerves and reduce the risk of postoperative complications. 3. To develop a technique for plasty of the anterior abdominal wall in mid-lateral postoperative hernias with a combination of retromuscular and subaponeurotic spaces. The researchers will compare an experimental group in which a new method of preparing the implant place will be used and a control group in which standard methods of treating postoperative ventral hernias were used to see whether the new method affects the improvement of the postoperative period and the reduction of complications.
Trial Details
NCT Number NCT05734222
Lead Sponsor Samara State Medical University
Conditions
(from sponsor)
Hernia, Ventral, Hernias Intestinal, Hernia Abdominal Wall
Related terms Hernia, Hernia, Abdominal, Hernia, Ventral, Surgical Wound
Enrollment 110 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov