Percutaneous Full-endoscopic Anterior Transcorporeal Cervical Discectomy: Surgical Design and Clinical Application

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR1900027820

Enrollment

Unknown

Registered

2019-11-30

Start date

2015-01-01

Completion date

Unknown

Last updated

2019-12-10

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

Conditions

cervical disc herniation

Interventions

Case series:surgery

Eligibility

Sex/Gender

All

Age

30 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. single-level central or paracentral CDH with soft herniation; 2. symptoms not improved after 3 months of standardized conservative treatment; 3. symptoms confirmed by relevant imaging examination; 4. herniated disc migration but without free

Exclusion criteria

Exclusion criteria: 1. lateral CDH; 2. lesions more than one segment; 3. herniated disc calcification, osteophytes present behind the vertebral body; 4. symptoms not consistent with imaging examinations; 5. free herniated discs in the spinal canal; 6. lesion segments with a history of surgery; 7. osteoporosis; 8. cervical instability.

Design outcomes

Primary

Measure	Time frame
Japanese orthopedic association scores;	—

Countries

China

Contacts

Public ContactXi Chen

Affiliated Hospital of Zunyi Medical University

2467607550@qq.com+86 17784920291

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026