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临床试验/CTRI/2025/02/080056
CTRI/2025/02/080056尚未招募4 期

A Prospective Randomized Comparision of Intravenous Paracetamol and Ibuprofen as Preemptive Analgesia in Total Laparoscopic Abdominal Hysterectomy

RNT Medical College Udaipur Rajasthan1 个研究点 分布在 1 个国家目标入组 88 人开始时间: 2025年2月20日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
88
试验地点
1
主要终点
Post operative analgesia

研究概览

简要总结

My clinical study is pre-emptive intravenous paracetamol and ibuprofen for acute post operative pain in laparoscopisc abdominal hysterectomy. We want to study comparative effect of paracetamol and ibuprofen infusion on post operative pain. Kindly consider it for CTRI registrar.

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
40.00 Year(s) 至 60.00 Year(s)(—)
性别
Female

入选标准

  • Patients of ASA grade I-II 2) Patients scheduled for laparoscopic abdominal hysterectomy surgeries.

排除标准

  • Lack of patient consent 2) Drug dependence 3) History of long-term NSAIDs and opioid analgesic use 4) Patients allergic to ibuprofen and paracetamol 5) Patients with diabetes or other neuropathic diseases 6) History of gastrointestinal bleeding, peptic ulcer or inflammatory bowel disease, asthma 7) Patients with severe hepatic or renal failure 8) Patients weighing less than 40 Kg.

结局指标

主要结局

Post operative analgesia

时间窗: 24 hours post-operatively

次要结局

  • 1)hemodynamic changes(2)the time to first analgesic requirement and total tramadol consumption)

研究者

发起方
RNT Medical College Udaipur Rajasthan
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Ravindra Kumar Gehlot

RNT Medical college Udaipur Rajasthan

研究点 (1)

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