Clinical study on the treatment of cervical spondylotic radiculopathy by unilateral double-channel spinal endoscope combined with endoscopic partial discectomy.

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500098767

Enrollment

Unknown

Registered

2025-03-13

Start date

2025-04-01

Completion date

Unknown

Last updated

2025-03-17

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

Conditions

Cervical spondylotic radiculopathy

Interventions

Observation group:Unilateral double-channel spinal endoscope combined with endoscopic partial discectomy

Control group: Anterior Cervical Discectomy and Fusion

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Cervical disc herniation with cervical central and lateral recess stenosis; 2. Cervical disc herniation with spinal stenosis within a single segment was diagnosed by imaging examination; 3. The clinical manifestations are typical symptoms and signs of nerve root compression of unilateral limb, and the VAS >=4 of the affected limb is >= 4; 4. After 3 months or more of regular and systematic non-surgical treatment, it is ineffective.

Exclusion criteria

Exclusion criteria: 1. Severe central cervical spinal stenosis; 2. Severe ossification of the posterior longitudinal ligament and cervical instability; 3. Patients with spinal infection or tumor have a history of major cervical trauma; 4. revision surgery at the same spinal level; 5.Complicated with serious basic diseases such as cardiovascular system diseases, liver and kidney dysfunction, respiratory system diseases, endocrine system diseases, etc.) can not tolerate surgery; 6. Coagulation dysfunction; 7. Combined with pathological changes of muscular nervous system or mental diseases; 8. Sepsis, hemorrhagic shock, electrolyte disorder and acid-base imbalance; 9. Patients with incomplete follow-up and missing clinical data; 10. Refuse to participate in this research.

Design outcomes

Primary

Measure	Time frame
Frequency of postoperative analgesic drugs used in two groups.;	—

Secondary

Measure	Time frame
Use of glucocorticoid;Neckdisabilityindex;Visual analogue scale;Operation time;Hematocrit;Drainage capacity of drainage tube;Postoperative skin edge necrosis;The occurrence of postoperative blisters;Days of hospitalization;Wear of neck brace in postoperative patients;Neck Disability Index;	—

Countries

China

Contacts

Public ContactShimin Li

Xuzhou Cancer Hospital

1019424569@qq.com+86 198 3451 9064

Outcome results

None listed

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