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Imaging and medium-term clinical efficacy analysis of the treatment of two different types of cervical radiculopathy with the assistance of posterior percutaneous endoscopic cervical discectomy

Imaging and medium-term clinical efficacy analysis of the treatment of two different types of cervical radiculopathy with the assistance of posterior percutaneous endoscopic cervical discectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600117172
Enrollment
Unknown
Registered
2026-01-20
Start date
2024-04-30
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Nerve-root type cervical spondylosis

Interventions

Intraspinal Segmental Cervical Spondylotic Radiculopathy N2:None
Foraminal Segment Cervical Spondylotic Radiculopathy N3:None

Sponsors

Lan Haiyang
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Symptoms of radiculopathy occur unilaterally in the neck, back, and arm, and conservative treatment has failed for more than six weeks.; (2) Unilateral single-level cervical disc lateral protrusion confirmed by MRI and CT, consistent with the patient's symptoms of CR; (3) Postoperative follow-up of at least 1 year, with complete clinical and imaging data

Exclusion criteria

Exclusion criteria: (1) Previous history of cervical spine surgery; (2) Isolated nerve root canal stenosis (confirmed by MRI and CT with no significant soft disc herniation), cervical spondylotic myelopathy or definite spinal instability or deformity; (3) History of malignant tumors, inflammatory joint diseases, trauma, mental disorders, and neuromuscular disorders.

Design outcomes

Primary

MeasureTime frame
The osteotomy rate of articular surface based on pre- and postoperative imaging findings;Neck Disability Index (NDI), Neck Pain Visual Analogue Scale (Neck-VAS), and Arm Pain Visual Analogue Scale (ARM-VAS) scores at Preoperative, Postoperative Day 3, Postoperative Month 3, Postoperative Month 6, and Postoperative Year 1;Radiological Parameters (SA-N, SA-F, SA-E, SA-ROM, AH, PH, AH/PH, CA-F, CA-E, CA-ROM, CDI) at Preoperative, Postoperative Day 3, Postoperative Month 3, Postoperative Month 6, and Postoperative Year 1;

Secondary

MeasureTime frame
Patient Demographics: Gender, Age, BMI, Smoking History, Diabetes History;Surgical Level, Preoperative Symptom Duration, Operative Time, Intraoperative Blood Loss, Average Length of Hospital Stay, Postoperative Complications, Postoperative Reoperation Rate, Macnab Outcome Criteria;

Countries

China

Contacts

Public ContactLan Haiyang

No. 10 Changjiang Branch Road, Daping, Yuzhong District

610957961@qq.com+86 136 6760 0047

Outcome results

None listed

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