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Percutaneous Full-Endoscopic Anterior Transcorporeal Decompression Versus Conventional Anterior Decompression and Fusion in Cervical Disc Herniation

The prospective study of percutaneous full-endoscopic anterior transcorporeal discectomy technique for cervical disc herniation

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027083
Enrollment
Unknown
Registered
2019-10-31
Start date
2013-12-01
Completion date
Unknown
Last updated
2019-11-04

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

Conditions

Cervical Intervertebral Disc Herniation

Interventions

experimental group:PEATCD
control group:ACDF

Sponsors

Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: Failure of strict conservative treatment; single-level central/mediolateral soft CIVDH; neurological symptoms were consistent with the results of radiological examinations; herniated disc fragment that migrated upward or downward but was not free; no evidence of instability in cervical spine; herniated disc at the segment C3-4 to C5-6 for PEATCD and C2-3 to C7-T1 for ACDF.

Exclusion criteria

Exclusion criteria: simultaneous cervical spinal canal stenosis; posterolateral herniation or foraminal stenosis; obesity; calcification of the herniated disc or posterior osteophytes of the vertebral body; previous operation at the same segment; herniation induced by trauma.

Design outcomes

Primary

MeasureTime frame
VAS;JOA;NDI;

Countries

China

Contacts

Public ContactWenbo Liao

Affiliated Hospital of Zunyi Medical University

wenbo900@sina.com+86 13985685360

Outcome results

None listed

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