Effectiveness of analgesia between nalbuphine and fentanyl in postoperative patients who underwent Laparotomy a randomized single blinded controlled trial

Dr Harsh P Chutke1 个研究点分布在 1 个国家目标入组 100 人开始时间: 2026年4月1日最近更新: 2026年3月12日

试验速览

阶段: 3 期
状态: 尚未招募
发起方
入组人数: 100
试验地点: 1

研究概览研究设计入排标准研究者研究点记录与标识符相似试验

研究概览

简要总结

This randomised single blinded study performed in our tertiary care centre will have hundred participants 50 in each group. group N will be given Nalbuphine and group F will be given fentanyl, These groups are made from the patients who underwent exploratory laboratory surgery and are in ICU for further management, we will compare the effectiveness of analgesia by seeing time taken to start first rescue analgesia, and also time taken for extubation after stoppage of sedation.

研究设计

研究类型: Interventional
分配方式: Randomized
盲法: Participant 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

•1 Age more than 18 years 2 Male or Female gender 3 ASA i or ii or iii 4 Patients undergoing elective/emergency laparotomy surgeries surgeries and coming to Surgical ICU for observation or for further management with MV support.

排除标准

•1 Patient refusal 2 Severe systemic illness , ASA iv 3 Patients on chronic opioid use 4 Intraoperative epidural or regional blocks 5 Allergy or hypersensitivity to drugs 6 Patients require prolonged ventilation ie 24 hrs.

研究者

发起方

Dr Harsh P Chutke

申办方类型

Private medical college

责任方

Principal Investigator

主要研究者

Dr Harsh Chutke (self)

Institute of Medical Sciences and SUM hospital

研究点 (1)

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