Multicenter clinical study of shock wave therapy after anterior cruciate ligament reconstruction

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400092905

Enrollment

Unknown

Registered

2024-11-26

Start date

2024-11-29

Completion date

Unknown

Last updated

2024-12-09

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

Conditions

None

Interventions

Experimental group:Conventional rehabilitation plus shock wave therapy

Control group:Conventional rehabilitation therapy plus simulated therapeutic head for shock wave therapy.

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients with anterior cruciate ligament injury who need anterior cruciate ligament reconstruction; 2. No other injuries such as fracture, blood vessel and nerve injury; 3. Unilateral anterior cruciate ligament rupture without other ligament or meniscus injury; 4. The age is 18-60 years old, and an informed consent form is required.

Exclusion criteria

Exclusion criteria: 1. Those who have cognitive impairment and cannot cooperate with rehabilitation exercise; 2. Complicated with serious cardiovascular and cerebrovascular diseases; 3. Those who use artificial ligament reconstruction.

Design outcomes

Primary

Measure	Time frame
Range of motion (ROM);International knee documentation committee(IKDC);	—

Secondary

Measure	Time frame
Pain visual analogue scale;Lysholm knee joint score;	—

Countries

China

Contacts

Public ContactSong Yufeng

The 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