To evaluate the availability of the remnant of rotator cuff after different injury time through molecular cytology and histological methods

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR1900024438

Enrollment

Unknown

Registered

2019-07-12

Start date

2018-02-02

Completion date

Unknown

Last updated

2019-07-15

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

Conditions

rotator cuff tear

Interventions

Grouped by different duration:N/A

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Clinical diagnosis of rotator cuff injury in patients.

Exclusion criteria

Exclusion criteria: 1. partial rotator cuff tear; 2. patients with infectious diseases like osteoarthritis and rheumatoid arthritis.

Design outcomes

Primary

Measure	Time frame
inducibility;	—

Countries

China

Contacts

Public ContactHuang Kai

Shanghai Sixth People's Hospital

huangkaiv5@163.com+86 18818273227

Outcome results

None listed

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