Optimization of Surgical Treatment of Patients With Postoperative Median and Median-lateral Ventral Hernias

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 25
Maximum Age: 88
Healthy Volunteers: f
View:

• The study will include patients with postoperative ventral hernias of median and lateral localization and an average hernial gate width from 4.1 to 15 cm (W2-W3 according to the EHS classification).. The size of the hernial gate is determined by CT.

Locations
Other Locations
Russian Federation
Clinics of Samara State Medical University
RECRUITING
Samara
Contact Information
Primary
Alexander Sonis, doctor
a.g.sonis@samsmu.ru
+79272024050
Backup
Vladislav Timoschuk, PhD student
v.v.timotshuk1@samsmu.ru
+79270004150
Time Frame
Start Date: 2022-09-29
Estimated Completion Date: 2025-05-23
Participants
Target number of participants: 110
Treatments
Active_comparator: Control Group
The control group is retrospective. It will include patients who have been operated on for POVG in the surgical department No. 1 of the KPH during the last 3 years (25-35) and 5-10 patients who will be operated on within the next 6-8 months.
Experimental: Established group
The established group - patients who will be operated on in the surgical department No. 1 of the KPH over the next 1.5 - 2 years, using the developed techniques.
Related Therapeutic Areas
Sponsors
Leads: Samara State Medical University

This content was sourced from clinicaltrials.gov