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High-energy extracorporeal shockwave therapy in patients with calcified rotator cuff tendinopathy

Effectiveness of high-energy extracorporeal shockwave therapy along with routine physical therapy on subjective and objective measures in patients with calcified rotator cuff tendinopathy; a randomized controlled trial

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200204046373N1
Enrollment
48
Registered
2020-03-28
Start date
2020-04-10
Completion date
Unknown
Last updated
2020-04-21

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

Conditions

Rotator cuff tendinopathy. Shoulder lesions

Interventions

Intervention 1: Intervention group: Shockwave therapy along with routine physical therapy. It will receive routine physical therapy treatment and high-energy extra-corporeal shockwave therapy. Routine

Sponsors

University of Lahore
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 55 Years

Inclusion criteria

Inclusion criteria: Patients with calcified rotator cuff tendinopathy referred by orthopedic surgeons or rheumatologists ofeither gender, age ranges from 30-55 years? Having at least 3 months history of shoulder pain located in the proximal lateral aspect of the upper arm Radiological evidence of type A or B calcification(=1cm or 10mm) 2 of 3 impingement test positive - Neer’s test, Hawkins tests and/or Jobe test

Exclusion criteria

Exclusion criteria: Patients having primary joint trauma or infection in shoulder region• Frozen shoulder or symptoms from cervical spine, glenohumeral osteoarthritis History of Shoulder instabilities, malignancies and nerve injuries, Chronic diabetic patients, diabetic neuropathy Patients with metallic implant, Pregnant female, Severe renal or cardiovascular diseases Patients having clotting disorders or having anticoagulant treatment History of any fracture or surgery in the shoulder complex or Full thickness rupture in the rotator cuff tendon

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Baseline, 6th and 12th week. Method of measurement: Numeric Pain Rating Scale.

Secondary

MeasureTime frame
Functional mobility. Timepoint: Baseline, 6 and 12 week. Method of measurement: Constant and Murley score.

Countries

Pakistan

Contacts

Public ContactArooj Fatima

University of Lahore

aruj43@hotmail.com+92 341 4391882

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 13, 2026