Optimization of Surgical Treatment of Patients With Incisional Ventral Hernias

Recruiting N/A Interventional Study
Hernia, Ventral Hernias Intestinal Hernia Abdominal Wall
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
25 – 88
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
110 (estimated)
Sponsor
Samara State Medical University · Other
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About This Trial
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, preperi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 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. Exclusion Criteria: * Pat…
Contacts

Alexander Sonis, doctor

+79272024050

a.g.sonis@samsmu.ru

CONTACT

Vladislav Timoschuk, PhD student

+79270004150

v.v.timotshuk1@samsmu.ru

CONTACT