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临床试验/CTRI/2024/04/066466
CTRI/2024/04/066466尚未招募2 期

An Interventional Study To Determine The Effectiveness Of Ultrasound Guided Needle Fenestration Of Coracohumeral Ligament For The Management Of Shoulder Adhesive Capsulitis In The Frozen Stage At Sawai Man Singh Medical College, Jaipur, Rajasthan

SMS MEDICAL COLLEGE JAIPUR1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年5月10日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
1. Shoulder pain and disability index for pain intensity and functional disability assessment

研究概览

简要总结

This study is a prospective, cohort ,intention to treat ,interventional clinical trial to evaluate the effectiveness and functional improvement in active ROM and passive ROM in patients with adhesive capsulitis in frozen stage treated with USG guided needle fenestration of the coracohumeral ligament using the shoulder pain and disability index scale.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Those willing to give informed written consent for participating in the study Patients with shoulder adhesive capsulitis in frozen stage Normal radiological appearance.

排除标准

  • The patient with poorly controlled Type 2 Diabetes mellitus or HbA1c more than 7.5 The patient with skeletal abnormality of Shoulder girdle or cervical thoracic spine Patient with any shoulder weakness secondary to Trauma And Spinal cord injury Patient with bleeding disorder INR more than 1.5 and platelet count less than 1 lakh per mm3 Patient currently with blood thinner eg warfarin etc The patient with history of shoulder fracture or rotator cuff injury Those with any other medical or surgical intervention that can interfere with the diagnosis or treatment protocol Allergy or intolerance to any drug or substance being used in the study.

结局指标

主要结局

1. Shoulder pain and disability index for pain intensity and functional disability assessment

时间窗: Before Intervention at the time of interview ,then follow up at baseline ,2 wks, 4 wks, 6 wks

2. Visual analog scale

时间窗: Before Intervention at the time of interview ,then follow up at baseline ,2 wks, 4 wks, 6 wks

3.The number of analgesics ingested per day

时间窗: Before Intervention at the time of interview ,then follow up at baseline ,2 wks, 4 wks, 6 wks

次要结局

未报告次要终点

研究者

发起方
SMS MEDICAL COLLEGE JAIPUR
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Rishab Bhagwan Meshram

SMS Medical College Jaipur

研究点 (1)

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