Actively Recruiting
Ultrasound-Guided Hydrodilatation With Triamcinolone Acetonide for Adhesive Capsulitis
Led by General Hospital of Ningxia Medical University · Updated on 2024-09-20
70
Participants Needed
1
Research Sites
42 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study was to compare the efficacy of ultrasus-guided hydrodilation of Rotator Cuff Interval combined with Posterior Glenohumeral recess approach and hydrodilation of the Rotator cuff Interval alone in Adhesive Capsulitis.
CONDITIONS
Official Title
Ultrasound-Guided Hydrodilatation With Triamcinolone Acetonide for Adhesive Capsulitis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older with clinical diagnosis of periarthritis of the shoulder
- Symptom duration longer than 1 month with shoulder range of motion limited in at least two directions (abduction less than 80°, flexion less than 130°, and rotation less than 30°)
- Completed plain radiographs, ultrasound images, and MRI to exclude secondary shoulder capsulitis before enrollment
You will not qualify if you...
- Secondary frozen shoulder caused by rotator cuff tear, calcifying tendinitis, osteoarthritis, infection, tuberculosis infection, rheumatic disease, or shoulder impingement syndrome
- Previous shoulder joint surgery
- Symptoms involving the cervical nervous system or abnormal nervous system findings
- Corticosteroid injection in the affected shoulder within the past 3 months
- Mental illness
- Contraindications to corticosteroid hormone use
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
General hospital of Ningxia medical university
Yinchuan, Ningxia, China, 750004
Actively Recruiting
Research Team
X
Xinli Ni, MD
CONTACT
P
Peng Ma
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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