Rehabilitation effect of shock wave on patients with humeral traumatic condylitis

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400084769

Enrollment

Unknown

Registered

2024-05-24

Start date

2024-05-30

Completion date

Unknown

Last updated

2024-07-08

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

Conditions

Lateral epicondylitis of humerus

Interventions

Experimental group:Conventional therapy plus shock wave therapy

Control group:Conventional therapy and simulated therapy head were used for shock wave therapy.

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-60 years old. 2. Patients diagnosed with lateral epicondylitis of humerus. 3. Patients who have not taken analgesic drugs in the past two weeks. 4. Patients who have no serious cardiopulmonary disease and can tolerate shock wave treatment.

Exclusion criteria

Exclusion criteria: 1. Patients with cognitive impairment. 2. Local skin damage or pathological damage. 3. Patients with severe cardiovascular and cerebrovascular diseases. 4. Patients with hematological diseases or other infectious diseases. 5. Those who are carrying out shock wave intervention or in the past three months.

Design outcomes

Primary

Measure	Time frame
Pain visual analogue scale;	—

Secondary

Measure	Time frame
Joint range of motion;American special hospital scoring system;	—

Countries

China

Contacts

Public ContactSong Yufeng

Second Hospital of Shanxi Medical University

songyufeng@sxmu.edu.cn+86 136 3347 5405

Outcome results

None listed

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