跳至主要内容
临床试验/CTRI/2025/11/097639
CTRI/2025/11/097639尚未招募2/3 期

ROBOTIC VERSUS LAPAROSCOPIC TRANS ABDOMINAL PRE-PERITONEAL REPAIR OF BILATERAL INGUINAL HERNIA : A RANDOMISED CONTROLLED TRIAL

not applicable1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2025年12月2日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
入组人数
48
试验地点
1
主要终点
To compare postoperative pain at 24 hours, 7 days, 1 month, 3 months and one year

研究概览

简要总结

Inguinal hernia repair is one of the most frequently performed surgical procedures globally,

accounting for over 20 million operations annually¹. The condition has a lifetime risk of

approximately 27% in men and 3% in women², making it a substantial contributor to surgical

workloads worldwide. Among these cases, bilateral inguinal hernias form a significant

subset, comprising up to 20–25% of all inguinal hernia presentations³. These cases are

inherently more complex, requiring bilateral dissection, longer operative times, and greater

attention to anatomical precision—particularly to avoid complications such as chronic groin

pain or recurrence.

Given these considerations, there is a pressing need for a prospective, study comparing both

economic and clinical outcomes between R-TAPP and L-TAPP in bilateral hernia repair. The

present study aims to address this by assessingpostoperative pain direct and indirect costs

andhernia recurrence using standardized methods in a tertiary care setting in India. By

generating data that integrates cost analysis with patient outcomes, this study will provide

valuable insights to inform surgical choice, guide institutional planning, and promote

evidence-based, cost-conscious healthcare delivery.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • 1 Adult patients aged from 18 to 65 years.
  • 2 Diagnosed with bilateral inguinal hernia (direct, indirect, or mixed) planned for elective minimally invasive repair.
  • 3 ASA physical status I and II 4 Willingness to undergo either robotic or laparoscopic TAPP repair as per allocation.

排除标准

  • Unilateral inguinal hernia.
  • Complicated hernias (for example obstructed, strangulated, incarcerated).
  • Inability or unwillingness to comply with follow up schedule.
  • Patients having any infectious or inflammatory disease condition pre-operatively .
  • Patient on chronic analgesic use
  • Concomitant malignancy.

结局指标

主要结局

To compare postoperative pain at 24 hours, 7 days, 1 month, 3 months and one year

时间窗: To compare postoperative pain at 24 hours, 7 days, 1 month, 3 months and one year | following surgery measured using the Visual Analog Scale (VAS)

following surgery measured using the Visual Analog Scale (VAS)

时间窗: To compare postoperative pain at 24 hours, 7 days, 1 month, 3 months and one year | following surgery measured using the Visual Analog Scale (VAS)

次要结局

  • To compare inflammatory stress response as measured by Serum CRP levels
  • To compare operative duration: Measured from skin incision to skin closure (in(minutes).)
  • To compare cost effectiveness(Intraop and followup at 3 m and 1 year)
  • To compare quality of life(at 3 months and one year following surgery)
  • To compare recurrence(at 3 months and one year following surgery)

研究者

申办方类型
Other [not applicable]
责任方
Principal Investigator
主要研究者

Nishant Ranjan

all india institute of medical sciences

研究点 (1)

Loading locations...

相似试验