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.
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