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临床试验/NCT07131527
NCT07131527已完成不适用

Comparative Study Between the Efficacy of Pre- Operative Oral Gabapentin Versus Diclofenac Sodium in Post-operative Analgesia in Adult Undergoing Laparoscopic Cholecystectomy

Sohag University2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年7月14日最近更新:
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
2
主要终点
the effect of preoperative oral Gabapentin versu Diclofenac sodium in adult patient undergoing laparoscopic cholecystectomy

研究概览

简要总结

this study amis to compare between perioperative oral Gabapentin versus Diclofenac sodium on postoperative analgesia patients undergoing laparoscopic cholecystectomy

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
20 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age from 20 to 60 years old. Both sexes. American Society of Anesthesiologists (ASA) physical status I- II. Patients undergoing laparoscopic cholecystectomy.

排除标准

  • Patients with hypertension. Pregnant women. Obese patients with BMI >35 kg/m
  • Alcoholics. Patients With DM Patient refusal

研究组 & 干预措施

group B will receive diclofenac sodium

Active Comparator

Patients included in this group will receive 100 mg diclofenac sodium 2 h before surgery.

干预措施: Diclofenac Sodium (Drug)

group A will receive oral Gabapentin

Active Comparator

Patients included in this group will receive 600 mg of gabapentin 2 h before surgery.

干预措施: Gabapentin (Drug)

结局指标

主要结局

the effect of preoperative oral Gabapentin versu Diclofenac sodium in adult patient undergoing laparoscopic cholecystectomy

时间窗: 8 hours after operation

postoperative pain by Numerical Rating Scale (0 represents "no pain" while 10 represents "the worst pain)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Manar Zakria Ismail

Resident , Anesthesia , Surgical Icu , Pain management Faculty of Medicine Sohag university

Sohag University

研究点 (2)

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