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临床试验/CTRI/2026/03/106032
CTRI/2026/03/106032尚未招募2/3 期

Efficacy of low dose dexmedetomidine as a perineural adjunct to ropivacaine for single shot interscalene brachial plexus block in arthroscopic shoulder surgery - A prospective randomized controlled study.

NAGIPOGU PRIYANKA1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2026年4月1日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
70
试验地点
1

研究概览

简要总结

Arthroscopic shoulder surgery is commonly associated with significant postoperative pain, which can affect early recovery and patient comfort. The interscalene brachial plexus block is considered the gold standard regional anesthesia technique for providing perioperative analgesia in shoulder surgeries. Ropivacaine is widely used for this block because of its long duration of action and favorable safety profile. However, the duration of analgesia with local anesthetics alone may be limited, leading to the need for additional postoperative analgesics. Dexmedetomidine, a highly selective alpha-2 adrenergic receptor agonist, has been increasingly used as an adjuvant to local anesthetics in peripheral nerve blocks. When administered perineurally, dexmedetomidine may prolong the duration of sensory and motor blockade, enhance the quality of analgesia, and reduce postoperative analgesic requirements. This prospective randomized controlled study aims to evaluate the efficacy of low-dose dexmedetomidine as a perineural adjunct to ropivacaine in single-shot interscalene brachial plexus block for patients undergoing arthroscopic shoulder surgery. The study will assess block characteristics, duration of postoperative analgesia, time to first rescue analgesic, total analgesic consumption, and incidence of adverse effects.

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 60.00 Year(s)(—)
性别
All

入选标准

  • Inclusion criteria : 1.Patients aged 18-60 years 2.Undergoing elective shoulder arthroscopic surgery under general anesthesia.
  • American Society of anesthesiologists(ASA) physical status, classification I or II, indicating those with no systemic disease or mild systemic disease.
  • 4.Ability to provide informed consent.

排除标准

  • Exclusion criteria: 1.History of allergy or hypersensitivity to dexmedetomidine.
  • Patients on antihypertensives such as methyldopa, clonidine, and other alpha2 agonists
  • Having BMI more than 30kg/m², peripheral neuropathy, coagulopathies, uncontrolled diabetes, liver and kidney dysfunctions
  • Participating in other clinical trials currently.

研究者

发起方
NAGIPOGU PRIYANKA
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr NAGIPOGU PRIYANKA

Nizams institute of medical sciences

研究点 (1)

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