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The study of low-temperature plasma nucleoplasty combined with collagenase in the treatment of cervical disc herniation

The study of low-temperature plasma nucleoplasty combined with collagenase in the treatment of cervical disc herniation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072523
Enrollment
Unknown
Registered
2023-06-15
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-06-18

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

Conditions

cervical disc herniation

Interventions

experimental group:low-temperature plasma nucleoplasty and collagenase chemonucleolysis
Control Group:low-temperature plasma nucleoplasty

Sponsors

Jiangwan Hospital, Hongkou District, Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Patients with single segment herniation who meet the diagnostic criteria for cervical disc herniation according to clinical symptoms, signs and CT/MRI examination; ? Recurrent cases after more than 3 months of conservative treatment; ?No severe spinal cord compression, no significant changes in spinal signals; ?The protruding nucleus pulposus tissue did not form free fragments and fell off in the spinal canal, but was still surrounded by fibrous annulus or posterior longitudinal ligament; ? The height of the intervertebral space is greater than 75% of normal.

Exclusion criteria

Exclusion criteria: ? Multi-segmental lesions and severe disease; ? Cervical dynamic position X-ray suggests spinal motor segment instability; ?CT showed calcification or ossification of the herniated intervertebral disc, hyperplasia of the foramina, intervertebral joint and uncinate joint, significant narrowing of the intervertebral space (less than half the width of the adjacent normal space), hypertrophy of the yellow ligament, cervical spinal stenosis (non-discogenic), and disc herniation or dissociation. ? Patients with severe disc degeneration on CT scan; ? Severe allergy.

Design outcomes

Primary

MeasureTime frame
VAS pain scores;

Secondary

MeasureTime frame
SF-36 Scale scores;Improved MacNab standard evaluation;Emotional assessment;Sleep assessment;

Countries

China

Contacts

Public ContactChan Zhu

Jiangwan Hospital, Hongkou District, Shanghai

13641686665@163.com+86 18121051678

Outcome results

None listed

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