Skip to content

Study on the curative effect of percutaneous endoscopic posterior cervical foraminotomy in the treatment of cervical and thoracic junction disc herniation

Study on the curative effect of percutaneous endoscopic posterior cervical foraminotomy in the treatment of cervical and thoracic junction disc herniation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097449
Enrollment
Unknown
Registered
2025-02-19
Start date
2025-02-23
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

Herniated disc at the cervicothoracic junction

Interventions

Sponsors

Weifang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Clinical signs and symptoms of cervical thoracic disc herniation (neurogenic pain or dysfunction due to compression or irritation of the cervical nerve roots); (2) Computed tomography (CT) and magnetic resonance imaging (MRI) revealed unilateral foraminal stenosis with cervical disc herniation; (3) Aged 20-80 years old; (4) The symptoms were not relieved after 3 months of conservative treatment; (5) Patients and their families sign informed consent after detailed understanding of the study content; (6) Did not participate in other clinical trials during the period; (7) At least 1 year of follow-up.

Exclusion criteria

Exclusion criteria: (1) Segmental instability (cervical motion beyond the normal physiological range) or severe cervical kyphosis (cervical spine abnormal kyphosis, generally greater than 30 degrees); (2) Combined with other spinal disorders, such as cervical spondylotic myelopathy, spinal tumors, and ossification of the posterior longitudinal ligament; (3) suffering from mental illness such as schizophrenia, drug dependence, mania and other inability to cooperate; (4) Previous cervical spine surgery history; (5) participating in other clinical trials; (6) The follow-up data were incomplete.

Design outcomes

Primary

MeasureTime frame
Neck Disability Index (NDI);Visual Analogue Scale (VAS);Japanese Orthopaedic Association(JOA)Scores;

Secondary

MeasureTime frame
EuroQol Five Dimensions Questionnaire(EQ-5D);Operation time;Intraoperative blood loss;Postoperative hospital stay;Perioperative complications;

Countries

China

Contacts

Public ContactWeiqiang Liu

Weifang People's Hospital

liuwqspine@126.com+86 187 6510 9800

Outcome results

None listed

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