Skip to content

Prospective multicenter randomized controlled trial of endoscopic anterior cervical discectomy decompression fusion (ACDF) and microscopic ACDF in the treatment of cervical spondylosis

Prospective multicenter randomized controlled trial of endoscopic anterior cervical discectomy decompression fusion (ACDF) and microscopic ACDF in the treatment of cervical spondylosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079612
Enrollment
Unknown
Registered
2024-01-08
Start date
2024-01-15
Completion date
Unknown
Last updated
2024-01-14

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

Conditions

cervical spondylosis

Interventions

microscope group:microscope
Endoscope group:Endoscope

Sponsors

The Seventh Affiliated Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Adult (=18 years old) ? Degeneration of the spinal cord caused by apparent compression of the spinal cord or nerve roots ? The severity of the disease does not cause the above conditions, but conservative treatment is ineffective for half a year or affects normal life and work ? radiculodynia is severe and does not respond to conservative treatment ? Neurotype cervical spondylotic disease caused by upper limb muscle weakness, atrophy, conservative treatment for 4-6 weeks failed

Exclusion criteria

Exclusion criteria: ? poor general condition, can not tolerate surgery ? The author of conservative treatment ? The possibility of pregnancy ? Active malignant disease: Patients with a history of malignant tumor must have been clinically cured and have no clinical signs or symptoms of malignant disease for at least 5 years ? Fracture, infection ? Under the age of 18 ? Participants in other spine-related studies ? Poor compliance, or failure to properly understand the fit to complete the interview

Design outcomes

Primary

MeasureTime frame
JOA scores;

Secondary

MeasureTime frame
Visual Analogue Scales(VAS);anterior intervertebral height (AIH);lordosis angle (LDA);operative time;blood loss;complications;cost-benefit ratio;quality of life changes;

Countries

China

Contacts

Public ContactTao Shu

The Seventh Affiliated Hospital, Sun Yat-sen University

shutao2019@126.com+86 186 2049 3159

Outcome results

None listed

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