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Efficacy of shock wave therapy in the treatment of tennis elbow in athletes using sonography

Efficacy of extracorporeal shock wave therapy in the treatment of lateral epicondylitis in athletes using ultrasonography

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190626044015N1
Enrollment
25
Registered
2019-08-04
Start date
2019-08-23
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Lateral Epicondylitis or Tennis Elbow. Lateral epicondylitis

Interventions

Intervention 1: Intervention group: a 4 Hz frequency shock wave, an energy flux density of 0.08 j/mm ², 2000 Shock, once a week for 3 weeks. Physical therapy is then performed with stretching exercis

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 36 Years

Inclusion criteria

Inclusion criteria: Diagnosed lateral epicondylitis At least 3 month of pain on lateral epicondyle Treatment to the affected area within the previous 3 month VAS above 4 Age between 2 and 4 years

Exclusion criteria

Exclusion criteria: < 18 year of age Contraindications for shockwave therapy ( malignancy, history of infected area involved, epilepsy, epilepsy, use of pacemaker, pregnancy) History of lateral epicondylitis surgery Elbow deformity Cervical radiculopathy History of rheumatology or polyarthritis The history of vasculitis The history of treatment with Shakviou in the last 12 months History of injection in the last 3 months (Corticosteroid, Autologous blood injection, PRP, Mesotherapy) Congenital or acquired deformities of the upper extremity

Design outcomes

Primary

MeasureTime frame
Measurement of tendon thickness. Timepoint: Before the intervention begins and one month after the end of the intervention. Method of measurement: Ultrasonography.

Secondary

MeasureTime frame
Pain score. Timepoint: At the beginning of the study (before the intervention), after the end of the intervention and one month after the end of the intervention. Method of measurement: Visual Analogue Scale.;Performance score. Timepoint: Before the intervention begins, after the intervention and one month after the end of the intervention. Method of measurement: Disabilities of the Arm, Shoulder, and Hand Questionnaire.;Hand strength score. Timepoint: Before the intervention begins, after the intervention and one month after the end of the intervention. Method of measurement: Dynamometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Atefeh Aminianfar

Semnan University of Medical Sciences

aminfar@semums.ac.ir+98 23 3365 4180

Outcome results

None listed

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