Optimization of Surgical Treatment of Patients With Incisional Ventral Hernias
Incisional Hernia, Medial Hernia, Medial-lateral Hernia
About this trial
This is an interventional treatment trial for Incisional Hernia focused on measuring Incisional Hernia, median, median-lateral, median-lateral Incisional hernia, hernia, Incisional
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: Patients without postoperative ventral hernias median and lateral localization
Sites / Locations
- Clinics of Samara State Medical UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Control Group
Established 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.
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.