Comparative Evaluation of Preoperative Preparation Methods in Patients With Large Incisional Hernias

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorState Budget Public Health Institution Scientific Research Institute - Ochapovsky Regional Clinical Hospital

About this trial

Patients with large, complex, or giant incisional hernias often require advanced preoperative optimization to facilitate safe abdominal wall reconstruction and reduce postoperative complications. Several strategies are currently used in clinical practice, including botulinum toxin A injection, progressive preoperative pneumoperitoneum, and their combination. However, the optimal differentiated approach based on hernia characteristics and abdominal wall tissue deficiency remains unclear.

This study aims to compare the effectiveness and safety of different preoperative preparation strategies in patients with large postoperative ventral hernias and loss of abdominal wall domain. Outcomes of patients receiving botulinum toxin A, progressive preoperative pneumoperitoneum, combined preparation, or no specific preparation will be analyzed.

The study will evaluate operative feasibility, ability to achieve fascial closure, postoperative complications, recurrence, and overall treatment outcomes.

Eligibility criteria

Qualifiers

Adults aged 18 years or older

Patients with ventral incisional hernia requiring elective surgical repair

Large and/or complex hernia defects requiring preoperative preparation

Ability to provide informed consent

Disqualifiers

Age under 18 years

Emergency surgery

Pregnancy

Contraindications to botulinum toxin A injection or progressive pneumoperitoneum

Trial design

Treatments tested in this trial

  • Botulinum Toxin A (Botox )
  • Progressive Preoperative Pneumoperitoneum
  • Combined Preoperative Preparation
  • Standard Preoperative Management

Treatment groups

120 Participants
are divided into 4 treatment groups