临床试验/CTRI/2023/03/050335

CTRI/2023/03/050335尚未招募不适用

Comparison between opioid free Anaesthesia and opioid Anaesthesia in Breast Cancer Surgery

Goa medical college and hospital1 个研究点分布在 1 个国家目标入组 60 人开始时间: 2023年9月3日最近更新: 2023年2月3日

适应症

试验速览

阶段: 不适用
状态: 尚未招募
发起方
入组人数: 60
试验地点: 1
主要终点: To compare the efficacy of Opioid Anaesthesia (OA) and Opioid free Anaesthesia (OFA) in reducing pain scores, postoperatively, in breast cancer surgery.

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The purpose of this trial is to compare the efficacy of opioid anaesthesia and opioid free anaesthesia in reducing pain scores, post operatively in breast cancer surgery

研究设计

研究类型: Interventional
分配方式: Other
盲法: Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围: 18.00 Year(s) 至 60.00 Year(s)（—）
性别: All

入选标准

•BMI: 18-25 ASA Status: I, II Surgery: Surgery for Cancer of Breast Informed Consent.

排除标准

•Pregnant& lactating women History of allergy to Dexmedetomidine, Lignocaine,Bupivacaine Patient on treatment with Beta blockers, HR< 50/min Epilepsy/ seizures Obstructive sleep apnea.

结局指标

主要结局

To compare the efficacy of Opioid Anaesthesia (OA) and Opioid free Anaesthesia (OFA) in reducing pain scores, postoperatively, in breast cancer surgery.

时间窗: VAS will be assessed at 0, 2, 4, 6, 12, 24 hours postoperatively

Pain will be assessed by visual analogue scale (VAS) score.

时间窗: VAS will be assessed at 0, 2, 4, 6, 12, 24 hours postoperatively

次要结局

To compare 1. Intraoperative hemodynamic parameters 2. Discharge time from Recovery Room 3. Duration of postoperative analgesia 4. Analgesia requirement in the postoperative period(Intraoperative parameters)

研究者

发起方

Goa medical college and hospital

申办方类型

Government medical college

研究点 (1)

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