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临床试验/NCT05528107
NCT05528107已完成不适用

Comparison of Laparoscopic Intraperitoneal Onlay Mesh (IPOM Plus) and Extended Totally Extraperitoneal (eTEP) Repair for Incisional Hernia - a Randomized Controlled Trial

City Clinical Hospital No.1 named after N.I. Pirogov2 个研究点 分布在 2 个国家目标入组 72 人开始时间: 2023年2月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
72
试验地点
2
主要终点
pain on postoperative day 1

研究概览

简要总结

The survey will compare primary and secondary outcomes of laparoscopic intraperitoneal onlay mesh (IPOM plus) and extended totally extraperitoneal (eTEP) repair for incisional hernia.

The research hypothesis is the following: patients who underwent eTEP repair may experience 30% less pain, assessed on the NRS-11 scale by the end of postoperative day 1, compared with IPOM plus procedure

详细描述

The use of minimally invasive surgery for the treatment of patients with incisional ventral hernias has significant advantages over open surgery. According to the current guidelines, the optimal technique for IPOM repair is a combination of suturing hernia defect and implantation an intraperitoneal anti-adhesive coated mesh prosthesis - the so-called "IPOM plus" technology (R.Bittner et al., 2019). The development of laparoscopic surgery has led to the new minimally invasive technique for ventral hernia repair - extended-view totally extraperitoneal plasty (eTEP) (I. Belyansky et al., 2018). An important advantage of eTEP is the non-fixation technique of implant placement due to correct positioning compared to the need for combined fixation for IPOM or IPOM plus, which probably affects on the level of postoperative pain in the early postoperative period.

The results of the first RCT comparing IPOM and eTEP ventral hernia repair were recently published (Mayank J. et al., 2022). It was demonstrated the benefits of eTEP repair in several aspects: less pain in the early postoperative period, as well as a faster return to physical activity and lower intervention costs. However, a significant limitation of this RCT is the analysis of interventions in a mixed group of patients with primary ventral and incisional hernias, as well as the use of IPOM procedure without suturing the hernia defect.

The sample size was determined based on the above hypothesis regarding the primary point of the study. Considering trial of Asencio F. et al. (2009) in a group of patients with incisional ventral hernias, the level of pain at the end of the first postoperative day after IPOM repair was 4.76 according to the VAS (visual analog scale) with a standard deviation of 1.975. Assuming α (type I error rate) 0.05, β 0.20, it would need a total sample size of 60 patients. Taking into account the probability of loss of patients in the evaluation of long-term results up to 20%, 72 patients will be required (36 patients per group).

Taking into account the inconsistency of the literature data on the level of pain in the early postoperative period after IPOM procedure for incisional ventral hernia repair, as well as the established primary point of the study, the investigators plan an additional calculation with correction of the sample size after evaluation intermediate results upon reaching 50% of enrolled patients of the initially established.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • midline incisional hernia
  • defect width 2-6 cm
  • ASA I-II class
  • Elective hernia repair
  • Considered eligible for minimally invasive ventral hernia repair
  • Able to give informed consent
  • Able to tolerate general anesthesia

排除标准

  • primary ventral herna
  • lateral hernia with/without midline
  • defect width more than 6 cm
  • refuse to give informed consent
  • prior mesh placement in the retrorectus space

研究组 & 干预措施

Laparoscopic Intraperitoneal Onlay Mesh plus ventral hernia repair

Active Comparator

Laparoscopic Intraperitoneal Onlay Mesh plus repair will be used to perform a minimally invasive ventral hernia repair with intraperitoneal mesh placement and suturing hernia defect.

干预措施: Lap IPOM plus (Procedure)

Extended-view totally extraperitoneal ventral hernia repair

Active Comparator

Extended-view totally extraperitoneal ventral hernia repair will be used to perform minimally invasive ventral hernia repair with retrorectus mesh placement

干预措施: eTEP (Procedure)

结局指标

主要结局

pain on postoperative day 1

时间窗: postoperative day 1

Pain score will be assessed using the Numeric Pain Rating Scale. The mean pain score is calculated between pain values at rest and on coughing. Participants verbally requested to rate their pain : "Rate your pain from 0 (no pain) to 10 (unbearable pain)". 0 point is the minimum and 10 point is the maximum. The higher the score, the more severe the pain.

次要结局

  • analgetic consumption(48 hours after surgery)
  • pain on postoperative days 7 and 30(postoperative 7 (±1) and 30 (±3) days)
  • length of stay(30 days after surgery)
  • number of participants with chronic pain(postoperative day 100 (±5 days))
  • postoperative complications(30 days after surgery)
  • pain 6 hours after surgery(6 hours (± 1 hour) after surgery)

研究者

发起方
City Clinical Hospital No.1 named after N.I. Pirogov
申办方类型
Other
责任方
Sponsor

研究点 (2)

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