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临床试验/CTRI/2025/09/094011
CTRI/2025/09/094011尚未招募不适用

A Randomized Controlled Trial to Evaluate the Efficacy of Intraperitoneal Instillation of Ropivacaine with Dexmedetomidine versus Bupivacaine with Dexmedetomidine for Postoperative Analgesia in Patients Undergoing Laparoscopic Cholecystectomy"

Dr Prakriti Choudhury1 个研究点 分布在 1 个国家目标入组 92 人开始时间: 2025年9月30日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
92
试验地点
1
主要终点
The time duration (in hours)

研究概览

简要总结

This randomized, double-blind clinical trial aims to compare the analgesic efficacy of intraperitoneal instillation of 0.25% bupivacaine versus 0.25% ropivacaine, both combined with dexmedetomidine (0.5 mcg/kg), in patients undergoing elective laparoscopic cholecystectomy. Conducted at KIMS, Bhubaneswar from August 2025 to July 2027, the study includes 92 ASA I/II patients aged 18–65 years. The primary outcome is the time to first rescue analgesia; secondary outcomes include total analgesic requirement, VAS pain scores, heart rate, and MAP over 24 hours. The study follows standardized anesthesia protocols and pain assessments.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator, Outcome Assessor and Date-entry Operator 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

  • ASA grade I or II Age between 18 and 65 years Hemodynamically stable Undergoing elective laparoscopic cholecystectomy Provided written informed consent.

排除标准

  • Emergency procedures Significant comorbidities (neurological, cardiac, respiratory, metabolic, hepatic, renal) Coagulation disorders Known allergy to study drugs.

结局指标

主要结局

The time duration (in hours)

时间窗: From the end of surgery (trocar removal) until the first patient request for rescue analgesia, within the first 24 hours postoperatively.

from the completion of

时间窗: From the end of surgery (trocar removal) until the first patient request for rescue analgesia, within the first 24 hours postoperatively.

surgery to the time patient

时间窗: From the end of surgery (trocar removal) until the first patient request for rescue analgesia, within the first 24 hours postoperatively.

requested for first rescue

时间窗: From the end of surgery (trocar removal) until the first patient request for rescue analgesia, within the first 24 hours postoperatively.

analgesic medication.

时间窗: From the end of surgery (trocar removal) until the first patient request for rescue analgesia, within the first 24 hours postoperatively.

次要结局

  • 1 .The total rescue analgesic(dose requirements in first 24)

研究者

发起方
Dr Prakriti Choudhury
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Prakriti Choudhury

Pradyumna Bal Memorial Hospital, Kalinga Institute of Medical Sciences

研究点 (1)

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