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The effect of high-power laser in the recovery of patients with rotator cuff tendinopathy

Comparing the effect of high-power laser and Meloxicam in improving shoulder joint function and pain of patients with rotator cuff tendinopathy

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200825048515N52
Enrollment
42
Registered
2022-05-12
Start date
2022-05-22
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Rotator cuff tendinopathy. Incomplete rotator cuff tear or rupture not specified as traumatic

Interventions

Intervention 1: Intervention group: After reducing the patient's pain, the patient is taught the exercises that strengthen the rotator cuff muscles and the shoulder girdle by repeating 3 times a day a

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with unilateral rotator cuff tendonitis Previous normal radiograph of the shoulder Age between 18 and 65 years Symptoms last less than 3 months Failure to perform any other therapeutic intervention during the last 3 months such as steroid injection into the shoulder joint or physiotherapy No contraindications to performing lasers Satisfaction to participate in the study

Exclusion criteria

Exclusion criteria: History of surgery Having a fracture near the shoulder Severe direct or indirect injuries following traction Generalized disorders of the musculoskeletal system or nervous disorders Having underlying diseases (including hypertension, coagulation disorders, heart disease, liver disease, kidney disease, cancer) drug abuse Inability to communicate and cognitive impairment

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before, immediately and three months after the intervention. Method of measurement: Visual Analog Scale (VAS).

Secondary

MeasureTime frame
Shoulder joint function. Timepoint: Before, immediately and three months after the intervention. Method of measurement: Disabilities of the Arm, Shoulder and Hand outcome Measure (DASH).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRazieh Maghroori

Esfahan University of Medical Sciences

maghroori@mui.ac.ir+98 31 3233 0091

Outcome results

None listed

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