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临床试验/CTRI/2024/08/072691
CTRI/2024/08/072691尚未招募4 期

Analysing the efficacy of periarticular shoulder injections in pain control after arthroscopic rotator cuff repair

MIOT International Hosptial1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2024年9月1日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
150
试验地点
1
主要终点
VAS pain score

研究概览

简要总结

Shoulder surgeries are one of the common orthopaedic procedures performed. With the increasing activity level of the younger population and overall survivorship, the requirement of various shoulder surgeries like the arthroscopic Bankart repair, Latarjet procedure, rotator cuff repair and reverse shoulder arthroplasty are on the rise. These surgeries, particularly arthroscopic rotator cuff procedures, are known to cause increased post-operative pain and discomfort to the patients. This affects the post-op physiotherapy, demoralises the patient, and increases the overall analgesic requirement. Pain-sensitive patients may require increased hospital stay increasing economic burden. Interscalene Brachial Plexus Block (ISB) has been a standard procedure to reduce pain following shoulder surgeries. But this procedure is not without complications. There is a good amount of learning curve associated with it. The administration of ISB requires sophisticated equipment like a sonogram. Phrenic nerve palsy, pneumothorax, persistent neurological symptoms and rebound pain are known complications of interscalene block. The alternatives include the suprascapular nerve block, superior trunk block, and intra-articular and periarticular injections. Periarticular Injections are emerging as effective alternatives to IBPB with similar efficacy as shown by some recent studies. The main objective of this study is to analyse the clinical effectiveness of periarticular injections in controlling post-operative pain following arthroscopic rotator cuff repair surgeries compared to interscalene block.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
30.00 Year(s) 至 90.00 Year(s)(—)
性别
All

入选标准

  • All patients with rotator cuff tear planned for arthroscopic cuff repair.

排除标准

  • Renal or liver compromise Asthmatic patients Glaucoma patients.

结局指标

主要结局

VAS pain score

时间窗: 3,12,24 and 48 hours post-surgery

次要结局

  • Analgesic requirement post-surgery(48 hours post surgery)

研究者

发起方
MIOT International Hosptial
申办方类型
Private hospital/clinic
责任方
Principal Investigator
主要研究者

Girinivasan Chellamuthu

MIOT International Hospital

研究点 (1)

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