A comparative evaluation of analgesic efficacy of intravenous paracetamol versus intravenous diclofenac as post-operative pain management in laparoscopic cholecystectomy- a prospective, comparative clinical study.
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 46
- 试验地点
- 1
- 主要终点
- To compare the analgesic effect and safety profile of intravenous paracetamol v/s intravenous diclofenac in
研究概览
简要总结
This study is to evaluate the analgesic efficacy of intravenous paracetamol and intravenous diclofenac as post-operative pain management in laparoscopic cholecystectomy in adult patients- A Comparative, Prospective, observational study to see which is superior in providing adequate post-operative analgesia safely without any adverse effects.
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •Patient willing to sign the written and informed consent.
- •Age group: 18-70 years.
- •Both male and female patients.
- •Patients posted for laparoscopic cholecystectomy under general anaesthesia with ASA-1 or ASA-2 grade.
排除标准
- •Patient’s refusal from taking part in the study.
- •Special populations.
- •Pregnant and lactating women.
- •History of allergy to drugs.
- •Severe kidney and liver disease.
- •Patients with neuropathies or nerve injuries.
- •Patients with pain due to cause other than presenting disease.
结局指标
主要结局
To compare the analgesic effect and safety profile of intravenous paracetamol v/s intravenous diclofenac in
时间窗: To study analgesic efficacy of intravenous paracetamol and intravenous diclofenac as post-operative pain management in laparoscopic cholecystectomy post-operatively at 30 minutes,4 hours, 8 hours, 12 hours, 24 hours.
post-operative pain management in laparoscopic cholecystectomy surgeries.
时间窗: To study analgesic efficacy of intravenous paracetamol and intravenous diclofenac as post-operative pain management in laparoscopic cholecystectomy post-operatively at 30 minutes,4 hours, 8 hours, 12 hours, 24 hours.
次要结局
- To study any intraoperative complications like nausea, vomiting, rigors, bradycardia, respiratory depression, hypotension.(Hemodynamic parameters will be recorded at)
研究者
Isha Jhatakia
Smt.Bhikiben Kanjibhai Shah Medical Institute and Research Centre