Improving surgical treatment for patients with ventral hernias
Optimization of Surgical Treatment of Patients With Postoperative Median and Median-lateral Ventral Hernias
This study is testing new surgical techniques for treating ventral hernias to see if they can reduce complications and help patients recover better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 110 (estimated) |
| Ages | 25 Years to 88 Years |
| Sex | All |
| Sponsor | Samara State Medical University Academic / other |
| Locations | 1 site (Samara) |
| Trial ID | NCT05734222 on ClinicalTrials.gov |
What this trial studies
This study aims to optimize the surgical treatment of postoperative ventral hernias by developing new surgical techniques. It focuses on understanding the anatomy of the abdominal wall to minimize damage to blood vessels and nerves during surgery. The researchers will compare the effectiveness of these new techniques in treating median and median-lateral hernias of medium to large sizes. The goal is to reduce postoperative complications and improve patient outcomes.
Who should consider this trial
Good fit: Ideal candidates are patients with median and lateral postoperative ventral hernias with hernial gate widths between 4.1 to 15 cm.
Not a fit: Patients without postoperative ventral hernias or those with hernias outside the specified size range may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to safer surgical options and better recovery for patients with ventral hernias.
How similar studies have performed: While there have been advancements in hernia repair techniques, this specific approach is novel and aims to address significant complications associated with current methods.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
Samara
- Clinics of Samara State Medical University — Samara, Russia (Recruiting)
Study contacts
- Principal investigator: Vladislav Timoschuk, Phd Student — Samara State Medical University
- Study coordinator: Alexander Sonis, doctor
- Email: a.g.sonis@samsmu.ru
- Phone: +79272024050
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.