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临床试验/NCT05094193
NCT05094193Unknown不适用

Trocar-site Infiltration With Ropivacaine Versus Tranversus Abdominis Plane Block Following Laparoscopic Cholecystectomy: a Double-blinded, Randomized-controlled Trial

Tunis University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年10月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
100
试验地点
1
主要终点
Acute postoperative pain

研究概览

简要总结

For symptomatic gall bladder disorders (cholelithiasis and cholecystitis), laparoscopic cholecystectomy (LC) has been considered as the gold standard treatment. However, these minimally invasive technique is associated with acute moderate pain during the 24 hours postoperative, which is routinely managed using opioids. The transversus abdominis plane (TAP) block has been used as part of a multimodal analgesia strategy. Besides, Wang et al found that TAP block is more effective than a conventional pain control, but not significatively different from another local incisional pain control that is port site infiltration.So, the aim of this study, is to compare the analgesic efficacy and safety of trocar-site infiltration with ropivacaine with ultrasound-guided TAP block following laparoscopic cholecystectomy when used as part of multimodal analgesia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • BMI < 30 kg/m2
  • Scheduled for laparoscopic cholecystectomy
  • ASA grade I, II and III

排除标准

  • Bile duct exploration, insertion of a T-drain or patients with acute cholecystitis
  • Conversion to open cholecystectomy or if the surgery exceeded 200 minutes
  • Severe systemic disease
  • Patients on analgesics for any reason
  • History of allergy to local anesthetics
  • An ongoing pregnancy
  • Patient refusal

结局指标

主要结局

Acute postoperative pain

时间窗: up to 24 hours

Visual analog scale (VAS) 0: "no pain" to 10: "severe pain" at rest and cough

Total opioid consumption

时间窗: Day 1

次要结局

  • Length of hospital stay(up to 1 week)
  • postoperative nausea and vomiting(Day 1)
  • Patient satisfaction and quality of recovery(Day 1)
  • Incidence of shoulder pain(Day 1)
  • Postoperative complication(up to 1 week)

研究者

发起方
Tunis University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Daghmouri Mohamed Aziz

Principal investigator

Tunis University

研究点 (1)

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