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The clinical application of nerve regeneration conduit

The clinical trial of nerve regeneration conduit in peripheral nerve injury

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-TNRC-10000801
Enrollment
Unknown
Registered
2010-03-03
Start date
2008-11-11
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

peripheral nerve injury

Interventions

Group A:small gap conduit to repair peripheral nerve injury
Group B:traditional epineurial neurorrhaphy to repair peripheral nerve injury

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Male and female aged 18 to 65 years old; 2. complex peripheral nerve injury; 3. gap between the two ruptured stumps was within 2-3mm after fully dissociation; 4. subjects or representative stipulated by laws had signed the informed consent

Exclusion criteria

Exclusion criteria: 1. Hypersensitiveness to chitin; 2. Nerve defect (cannot be connected after fully dissociation); 3.dysfunction in heart, lung, liver or kidney; 4. Obsolescence peripheral nerve injury; 5. Pathological peripheral nerve injury; 6. Acute or chronic infection; 7. Dyscrasia result from chronic wasting disease and cannot tolerate operation; 8. Patients whose treatment and assessment may be affected this research plan.

Design outcomes

Primary

MeasureTime frame
The clinical assessment of functional recovery(sensory and movement);sensory and motor nerve conduction velocity;

Countries

China

Contacts

Public ContactBaoguo Jiang
jiangbaoguo@vip.sina.com+86 010 88326558

Outcome results

None listed

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