Skip to content

"Hydrodilatation in adhesive capsulitis", " Intra-articular corticosteroid in adhesive capsulitis"

A Comparative study between intra-articular corticosteroid injection and ultrasound-guided hydrodilatation in patients with shoulder adhesive capsulitis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210910052428N1
Enrollment
48
Registered
2021-10-12
Start date
2021-11-20
Completion date
Unknown
Last updated
2021-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Shoulder adhesive capsulitis. Adhesive capsulitis of unspecified shoulder

Interventions

Intervention 1: Intervention group: injection of normal saline 0.9% with 25cc/sec rate in prevention of capsular rupture due to large amount injection, with injection of 3cc lidocaine under sterile ci

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Presence of pain and shoulder range of motion limitation more than 30 degree in more than two motion plane Presence of pain and shoulder range of motion limitation more than one month

Exclusion criteria

Exclusion criteria: Shoulder pain after cerebrovascular attack in paretic side Patients with severe glenohumeral joint osteoarthritis Patients with complete rotator cuff ligaments tear Immune deficiency Fracture in humerus bone or scapula Pregnant women Patients with cancer History of allergy and reaction due in use drugs Shoulder joint rheumatoid arthritis Severe depression Uncontrolled diabetes

Design outcomes

Primary

MeasureTime frame
" Score of pain in visual analoge scale questionnaire" , " Shoulder disability score in shoulder pain and disability index questionnaire". Timepoint: " Measurement of shoulder range of motion and pain score at the beginning, 2, 4 and 8 weeks after shoulder injection". Method of measurement: Visual analog scale and shoulder pain and disability index.

Secondary

MeasureTime frame
Shoulder Pain. Timepoint: Before intervention; two weeks, four weeks and eight weeks later. Method of measurement: Visual Analogue Scale; Shoulder Pain And Disability Index.;Shoulder range of motion. Timepoint: Before intervention; two weeks, four weeks and eight weeks later. Method of measurement: With usage of goniometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVahide Nadgaran

Shiraz University of Medical Sciences

v.nadgaran@gmail.com+98 71 3722 2038

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026