跳至主要内容
临床试验/CTRI/2024/08/072176
CTRI/2024/08/072176尚未招募不适用

Comparing Superior trunk of brachial plexus block and supraclavicular nerve block with shoulder pericapsular blocks and supraclavicular nerve block for post operative analgesia in patients undergoing shoulder arthroscopic surgeries.

Antrofelix M1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年7月14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
80
试验地点
1
主要终点
To assess the postoperative pain scores between the two groups using Visual Analogue pain assessment Scale (VAS).

研究概览

简要总结

Arthroscopicshoulder surgeries have the potential to cause severe postoperative pain.  Poor pain management leads to poor outcomes, with longer hospital stay and delayed functional recovery.  It also can cause an inability to participate in rehabilitation programs, leading to poor quality of life for the patients. Shoulder surgeries are amenable to either general anesthesia, regional anesthesia, or regional anesthesia with sedation. Opioid analgesics are commonly used for analgesia when nerve blocks are not used. Opioids are effective in relieving postoperative pain at rest but may increase post operative nausea and vomiting, somnolence, constipation, urinary retention, respiratory depression, and sleep disturbances. The interscalene brachial plexus block (ISB) has been reported to provide excellent post-operative analgesia but can produce side effects like phrenic nerve blockade resulting in diaphragmatic paresis causing respiratory distress to the patient. This necessitates the search for other nerve blocks which has similar analgesic efficacy as the ISB but without any associated complications. Injection around the superior trunk of the brachial plexus is an alternative technique that may reduce this risk. Along with supraclavicular block was suggested to provide effective anesthesia for shoulder surgery with a low rate of side-effects. The aim of this study is to compare the shoulder pericapsular blocks with superior trunk of brachial plexus block in relieving postoperative shoulder pain, intraoperative hemodynamic stability, avoiding motor block and allowing in early rehabilitation.

Patients undergoing shoulder surgeries will be randomized into 2 groups as

group A- will receive superior trunk of Brachial plexus block with supraclavicular nerve block.

group B- will receive shoulder capsular blocks with supraclavicular nerve block

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 80.00 Year(s)(—)
性别
All

入选标准

  • ASA I, II, III undergoing elective shoulder surgery.

排除标准

  • ASAV IV, Patient refusal, Deranged coagulation profile, Local Anesthestic Allergy, Neuropathy.

结局指标

主要结局

To assess the postoperative pain scores between the two groups using Visual Analogue pain assessment Scale (VAS).

时间窗: 36 hours

次要结局

  • To assess the requirement of rescue analgesia, intraoperative hemodynamic stability, motor blockade.(24 hrs)

研究者

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

Antrofelix M

christian medical college

研究点 (1)

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