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Clinical Study of Polyester Artificial Ligament

Clinical Study of Polyester Artificial Ligament

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17010366
Enrollment
Unknown
Registered
2017-01-09
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Ligament Injury

Interventions

polyester artificial ligament:using polyester artificial ligament
Ohter artificial ligament:use ohter artificial ligament

Sponsors

Shanghai Chest Hospital, Shanghai Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years; 2. Coracoclavicular ligment injured ; 3. Annular ligament injured; 4. Achilles tendon injured 5. Having read the subject's instructions, agreed to enter the group and signed ICF.

Exclusion criteria

Exclusion criteria: 1. Fractures 2. More than one ligament injured. 3. Reject to sigh the ICF.

Design outcomes

Primary

MeasureTime frame
Time of the patient to be able to walk depended by walking stick;Lysholm scores;—

Countries

China

Contacts

Public ContactZhou Mingzhou

Shanghai Chest Hospital, Shanghai Jiaotong University

zmzcloudy@sina.com+86 18016388662

Outcome results

None listed

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