跳至主要内容
临床试验/CTRI/2023/08/056577
CTRI/2023/08/056577尚未招募4 期

To compare post operative pain and rescue analgesic requirement in patients undergoing laparoscopic transabdominal pre peritoneal (tapp) and laparoscopic totally extra peritoneal (tep) approach for inguinal hernias

Max super speciality hospital1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2023年8月30日最近更新:

试验速览

阶段
4 期
状态
尚未招募
入组人数
50
试验地点
1
主要终点
To assess and compare post operative pain of group A (tep repair) and group B (tapp repair)

研究概览

简要总结

This study is a prospective, consecutive, non randomised, non blinded, observational study that will be organised and carried out in the department of  anesthesiology and pain management, Max super speciality hospital, Mohali, Punjab with due authorisation from the Institutional Ethics Committee and Review Board and in compliace to informed, written consents taken from the patients. This study will assess and compare the postoperative pain, need for additional analgesics postoperatively, incidence of postoperative nausea and vomiting, sites of pain, duration of hospital stay, and patient satisfaction among patients undergoing laparoscopic totally extra peritoneal (tep - group A) repair and laparoscopic transabdominal pre peritoneal (tapp - group B) repair for inguinal hernias.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • Patients aged more than or equal to 18 years
  • Patients with ASA status I, II, III
  • Patients capable of providing a written, informed consent.

排除标准

  • Patient refusal
  • Patients having a history of chronic pain and analgesic requirement
  • Any surgery converted to open surgery
  • Patients with recurrent inguinal hernias
  • Patients with a previous history of abdominal surgery
  • Patients with complicated hernias.

结局指标

主要结局

To assess and compare post operative pain of group A (tep repair) and group B (tapp repair)

时间窗: At 1 hour, 6 hours, 12 hours, 24 hours postoperatively and on OPD follow up visit post discharge

次要结局

  • To compare -(1. The need for additional analgesic requirement)

研究者

申办方类型
Private hospital/clinic

研究点 (1)

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