Clinical study of extracorporeal shock wave on joint dysfunction after rotator cuff degeneration repair

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000032355

Enrollment

Unknown

Registered

2020-04-26

Start date

2020-05-01

Completion date

Unknown

Last updated

2020-04-27

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

Conditions

rotator cuff degeneration

Interventions

Group 1:exercise therpry+interferencial currents

Group 2:shockwave+exercise therpry+interferencial currents

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Aged 50-70 years; 2. According to diagnosis of rotator cuff injury and underwent arthroscopic rotator cuff repair; 3. 6-8 weeks after surgery; 4. Good compliance, normal cognitive understanding, can cooperate Carry out relevant treatment; 5. The patient himself signs the informed consent.

Exclusion criteria

Exclusion criteria: 1. Rotator cuff injury combined with fracture; 2. A clear history of trauma; 3. People with heart disease, severe hypertension, and skin ulceration at the treatment site who cannot be treated with extracorporeal shock wave.

Design outcomes

Primary

Measure	Time frame
CMS;the university of California at Los Angeles shoulder rating scale;VAS;ROM;	—

Countries

China

Contacts

Public ContactWeiwei Zhu

Xuzhou Rehabilitation Hospital

1057403497@qq.com+86 13775884856

Outcome results

None listed

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