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临床试验/NCT07169006
NCT07169006尚未招募不适用

The Effect of Preoperative Gabapentin on Postoperative Pain Control and Analgesic Requirements Following Bariatric Surgery

Ain Shams University0 个研究点目标入组 102 人开始时间: 2026年1月1日最近更新:
干预措施
相关药物

试验速览

阶段
不适用
状态
尚未招募
入组人数
102
主要终点
Comparing pain score between the two groups during 1st postoperative 24 hours using visual analogue score (VAS

研究概览

简要总结

The importance of bariatric anesthesia and analgesia research cannot be ignored as it can inform and improve the perioperative protocols for other patients with morbid obesity irrespective of the surgical procedures they are undergoing

详细描述

Among various postoperative complications, pain is the main adverse event experienced by patients. Good control of postoperative pain is an important factor for reducing early postoperative complications such as pulmonary embolism, deep vein thrombosis, ileus, and respiratory infections, and for decreasing length of stay, lowering costs, and increasing patient satisfaction

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

盲法说明

Single

入排标准

性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • patients with impaired liver or kidney disease
  • patients with history of hypersensitivity to gabapentin
  • patients with history of alcohol abuse, chronic pain or frequent use of analgesic
  • patients with uncontrolled medical disease

研究组 & 干预措施

Group 1

Experimental

Will receive a single dose of gabapentin 300 mg preoperatively before standard general anesthesia

干预措施: Group 1 (Drug)

Group 2

Placebo Comparator

will receive a placebo before standard general anesthesia

干预措施: Group 2 (Drug)

结局指标

主要结局

Comparing pain score between the two groups during 1st postoperative 24 hours using visual analogue score (VAS

时间窗: 24 hours postoperative

Comparing pain score between the two groups during 1st postoperative 24 hours using visual analogue score (VAS

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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