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临床试验/CTRI/2026/03/105546
CTRI/2026/03/105546尚未招募不适用

OPTIMAL DEXEMEDETOMIDINE DOSAGE FOR INTERSCALENE BLOCK IN ARTHROSCOPIC SHOULDER SURGERY FOR INTRA-OPERATIVE SURGICAL CONDITION AND POST-OPERATIVE ANALGESIA

Kasturba Medical College1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年4月28日最近更新:

试验速览

阶段
不适用
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 prospective observational study will be conducted at Kasturba Medical College Hospitals, Mangalore (KMC Attavar, UMC Ambedkar Circle, and Govt Wenlock Hospital) to determine the optimal dose of dexmedetomidine as an adjuvant in ultrasound-guided interscalene brachial plexus block for patients undergoing arthroscopic shoulder surgery under general anaesthesia.

Adult patients aged 18–60 years, ASA I–II, scheduled for arthroscopic shoulder surgery will be included. Participants will be grouped based on the dose of dexmedetomidine administered in the interscalene block:

  • Group A: 0.5 mcg/kg dexmedetomidine
  • Group B: 1 mcg/kg dexmedetomidine

The primary outcomes will be intra-operative surgical field condition score and post-operative analgesia assessed using VAS score (including time to first rescue analgesia). Secondary outcomes include hemodynamic parameters (HR, SBP, DBP, MAP) and the requirement of vasopressors (ephedrine/mephentermine) and atropine.

The study aims to identify the dose providing better surgical field conditions, hemodynamic stability, and prolonged post-operative analgesia, thereby improving perioperative outcomes in shoulder arthroscopy.

研究设计

研究类型
Observational

入排标准

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

入选标准

  • Patients requiring any arthroscopic shoulder surgery.

排除标准

  • Patients unwilling to participate in the study.
  • Patients with contraindications to Regional Anaesthesia.
  • Patients with known allergy to local anaesthetics 4) Patients with American Society of Anaesthesiology (ASA) Grade III or higher.

研究者

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

Dr Yagya Bikram Basnett

Kasturba Medical College

研究点 (1)

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