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临床试验/CTRI/2026/01/100662
CTRI/2026/01/100662尚未招募2/3 期

Evaluation of dexamethasone as an adjuvant for scalp nerve block for post operative analgesia following supratentorial craniotomy

pt. B.D. Sharma PGIMS Rohtak1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年1月20日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
入组人数
60
试验地点
1

研究概览

简要总结

This study is to evaluate the role of dexamethasone as adjuvant added to scalp nerve blocker postoperative analgesia following supratentorial craniotomy. Depending on whether Dexamethasone is used as adjuvant to provide postoperative analgesia following  craniotomy, patients will be randomly allocated into two groups. Group S will include patient receiving drug alone while Group DS will receive dexamethasone along will drug ,10 min prior to surgery. Primary objective will be to compare Visual Analogue Scale for pain following Scalp nerve block, Secondary objective will be intraoperative heamodynamic parameter, duration of postoperative analgesia ,24hrs analgesic requirement. demand of first rescue analgesia ,post operative nausea and vomiting, drug related complication if any.Data will be compiled and appropriate stastical test will be used to analyse the results

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
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • American society of anaesthesiologist physical status classification 1-3, Glassgow coma scale(GCS) score of 15/15 schedule to undergo elective supratentorial craniotomy under general anaesthesia.

排除标准

  • Patients having contraindications to regional anaesthesia 2)coagulation abnormalities 3)active infection at injection site 4)chronic pain syndromes 5)chronic opioid use(more than 2 weeks or 3 days per week for more than 1 month) 6)extreme body mass index(<15 or >35) 7)refusal or inability of patient or legal guardian to provide inform consent.

研究者

申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Kirti Kshetrapal

pt. B.D. Sharma PGIMS Rohtak

研究点 (1)

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