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Carticosteroid injection combined with mobilization versus mobilization alone in sub acromial impingement syndrome.

Comparative effects of Carticosteroid injection combined with mobilization versus mobilization alone in sub acromial impingement syndrome. â?? Randomized, placebo control trial.

Status
Unknown
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/025692
Enrollment
60
Registered
2020-06-08
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M95- Other acquired deformities of musculoskeletal system and connective tissue

Interventions

Intervention1: Carticosteroid injection combined with mobilization: Carticosteroid injection: In intra articular carticosteroid injection application patients will be treated with a posterior approa

Sponsors

Prince Sattam Bin Abdulaziz University Al Kharj Saudi Arabia
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: male volley ball players, age group of 18â??25 years, clinical diagnosis of sub acromial impingement syndrome by an orthopedic surgeon, pain localised to the proximal anterolateral shoulder region, positive for pain on at least one of the following three impingement tests: Hawkins-Kennedy, Neerâ??s, Jobeâ??s and (iv) positive for pain on at least one of the following four tests: painful arc, drop arm test, lift-off test, and resisted external rotation.

Exclusion criteria

Exclusion criteria: large, full-thickness rotator cuff tear, history of previous injury around shoulder, severe labrum or capsule tear, moderate-severe glenohumeral or acromioclavicular joint osteoarthritis, glenohumeral joint instability including previous shoulder dislocation/subluxation, neurological deficits of the upper limb patient with radiating pain, severe pain around the shoulder or neck pain, skin infections. history of Fracture around shoulder complex,

Design outcomes

Primary

MeasureTime frame
Pain intensity â?? VAS Pain pressure threshold (PPT) Active and passive abduction (in the frontal plane) and external rotation (with the arm at 0 degrees of abduction) ROM Functional disability â?? SPADI Timepoint: At baseline, after 4 weeks, 8 weeks and 6 months follow up.—

Secondary

MeasureTime frame
MRI: Coracohumeral interval (space between the tip of the coracoid and the humerus) Thicknesses of supraspinatus tendon tear US: Thickness of the subacromial-subdeltoid bursa Timepoint: At baseline, after 4 weeks, 8 weeks and 6 months follow up.—

Countries

Saudi Arabia

Contacts

Public ContactGopal Nambi

Prince Sattam Bin Abdulaziz University

physio_gopal@rediffmail.com00966501878382

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 5, 2026