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Clinical Effect Study of Blood Flow Restriction Training Combined with Extracorporeal Shock Wave Therapy for Tennis Elbow

Clinical Effect Study of Blood Flow Restriction Training Combined with Extracorporeal Shock Wave Therapy for Tennis Elbow

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116077
Enrollment
Unknown
Registered
2026-01-05
Start date
2026-01-12
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Tennis Elbow

Interventions

Experimental group:Blood Restriction Training with Extracorporeal Shock Wave
Control group:No-Blood Restriction Training with Extracorporeal Shock Wave

Sponsors

The First Medical Center of Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age 18–60 years, any gender; 2. Diagnosed with tennis elbow, with symptoms lasting more than 2 weeks. Diagnosis is based on the following criteria: tenderness at the lateral epicondyle of the humerus; positive Cozen test, Maudsley test, and/or Mill test; grip strength decrease >10% (elbow extended vs. elbow flexed); 3. Able to understand and actively participate in the training program, and agrees to sign this clinical study informed consent form.

Exclusion criteria

Exclusion criteria: 1. History of ipsilateral shoulder tendinopathy, cervical radiculopathy, rheumatoid arthritis, neurological deficits, radial nerve entrapment, etc.; 2. Recent (=6 months) intervention treatments (such as corticosteroid injections); 3. History of lateral epicondylitis in the ipsilateral elbow within the past 2 years; 4. Coexisting severe cardiovascular disease; 5. Upper limb orthopedic surgery or history of deep vein thrombosis within the past 6 months; 6. Body mass index (BMI) >30; 7. History of malignant tumors; 8. Investigator assessment that the patient has poor compliance and cannot complete the study as required; 9. Other contraindications or complications that may affect training.

Design outcomes

Primary

MeasureTime frame
Numeric Pain Rating Scale, NPRS;PRTEE questionnair;Painless grip strength;

Secondary

MeasureTime frame
Isometric muscle strength of the elbow flexor/extensor muscles;Thickness of the triceps brachii tendon;

Countries

China

Contacts

Public ContactWang Gang

The First Medical Center of Chinese PLA General Hospital

301wanggang@sina.com+86 134 2644 9200

Outcome results

None listed

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