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Comparison of subacromial Ketorolac, betamethazone LA and triamcinolon injection in treatment of impingement syndrome

Comparison of subacromial Ketorolac, betamethazone LA and triamcinolon injection in treatment of impingement syndrome

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017042927797N2
Enrollment
105
Registered
2017-06-07
Start date
2016-10-03
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Impingement syndrome of shoulder. Impingement syndrome of shoulder

Interventions

Intervention 1: In Group A subacromial ketorolac injection with a posterior approach will be done. Intervention 2: In Group B subacromial Triamcinolon injection with a posterior approach will be done.
Treatment - Drugs
In Group A subacromial ketorolac injection with a posterior approach will be done.
In Group B subacromial Triamcinolon injection with a posterior approach will be done.
In Group C subacromial Betamethazon LA injection with a posterior approach will be done.

Sponsors

Vice Chancellor of Reaserch and Technology, Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: all people with shoulder pain referred to orthopedic clinics and diagnostic imaging in the diagnosis of shoulder impingement syndrome has been laid for them and their consent to participate in the study. Exclusion criteria: patients with all of the diagnosis except impingement syndrome; Do not go to the next follow up; do not have a history of shoulder dislocation or fracture or a systemic disease that affects the joint and soft tissue .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Determine the function of the patient. Timepoint: Before injection, weeks 2, 4 and 6 after injection. Method of measurement: By Oxford Shoulder Score questionnaire.;Patient pain severity. Timepoint: Before injection, weeks 2, 4 and 6 after injection. Method of measurement: By Visual Analogus Scale questionnaire.

Secondary

MeasureTime frame
Tendon Rupture. Timepoint: weeks 2, 4 and 6 after injection. Method of measurement: Physical Examination.;Injection site infection. Timepoint: weeks 2, 4 and 6 after injection. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Hamed Abolhassani

Babol University of Medical Sciences

bcrdc90@yahoo.com+98 11 3219 7667

Outcome results

None listed

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