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A comparative study of the effectiveness of two treatment methods, dry needling and kinesiotaping, in the treatment of tennis elbow

A comparative study of the effectiveness of two treatment methods, dry needling and kinesiotaping, in the treatment of tennis elbow

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230722058889N1
Enrollment
62
Registered
2023-09-23
Start date
2023-08-11
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

lateral epicondilitis. Lateral epicondylitis

Interventions

Intervention 1: Intervention group: Dry needling method:The first group is treated with dry needling and exercise and a non-steroidal anti-inflammatory drug (Meloxicam 15 mg daily) for three weeks. Th

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age 30 to 65 years Pain in the lateral epicondyle for at least a month Pain in cozen's test Pain in the extensor carpi radialis test (that is, resistance to the extension of the middle finger - Maudsley's test) Supination resistance test (Mill's test)

Exclusion criteria

Exclusion criteria: Diabetes Mellitus Cervical radiculopathy Bilateral lateral epicondylitis neuropathy Arthritis in the upper limb or a history of arthritis Bilateral lateral epicondylitis pregnancy History of forearm and elbow surgery Acute elbow trauma Allergy to Kinesiology tape Cubital tunnel syndrome Carpal tunnel syndrome autoimmune disease Rotator cuff tendonitis Local or systemic upper limb infection Fibromyalgia syndrome Medial epicondylitis of the same side An old fracture in the damaged arm Changing the shape of the elbow Coagulation diseases

Design outcomes

Primary

MeasureTime frame
Pain score. Timepoint: Before performing the treatment methods and in the 3rd and 8th weeks after the treatment. Method of measurement: Visual Analogue Scale.;Functional status. Timepoint: Before performing the treatment methods and in the 3rd and 8th weeks after the treatment. Method of measurement: Patient Rating Forearm Evaluation Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRazieh Maghruri

Esfahan University of Medical Sciences

ramaghroori@yahoo.com+98 31 3668 5555

Outcome results

None listed

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