A Comparative Study of Range of Motion of Shoulder between Ultrasound Guided Hydrodilatation with Corticosteroid and Conventional Corticosteroid Injection alone in Adhesive Capsulitis: A Randomized, Controlled and Double-blinded Study

Phase 1

Recruiting

• Conditions: adhesive capsulitis patient with not improve by physical therapy; ultrasound; adhesive capsulitis; hydrodilatation

• Registration Number: TCTR20210217005
• Lead Sponsor: /A

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-02-17
• Study Completion: 2023-12-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 52

Inclusion Criteria

1. patient with adhesive capsulitis who limit of passive motion greater than 30 degree in two planes of movement.
2. age > 18 years
3. patient who received physical therapy more than 1 month and has NPRS at least 4
4. Graduated elementary school or can read Thai language

Exclusion Criteria

1. previous steroid injection to shoulder joint or manipulation under general anesthesia
2. they had any of the following calcification of the rotator cuff, rotator cuff tear,
disorders of the biceps tendon or acromioclavicular joint.
3. secondary adhesive capsulitis ex. cancer, rheumatoid arthritis, infectious arthritis, stroke or fracture
4.uncontrolled diabetes
5. major depression
6. bleeding disorder
7. allergic to steriod, lidocaine or normal saline

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Shoulder range of motion at6 weeks after end of the intervention goniometer

Secondary Outcome Measures

Name	Time	Method
Patient reported outcome before and after 1,6 weeks after intervention the Thai version of the Shoulder Pain and Disability Index, Thai SPADI),Patient reported outcome before and after 1,6 weeks after intervention the Thai version of the Oxford Shoulder Score, OSS-TH,pain before and after 1,6 weeks after intervention NPRS