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The clinical efficacy of low energy laser disc decompression on treatment of cervical disc herniation

The clinical efficacy of low energy laser disc decompression on treatment of cervical disc herniation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-17010356
Enrollment
Unknown
Registered
2017-01-08
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

cervical disc herniation

Interventions

treatment goup:Low - energy Laser Decompression of Intervertebral Disc

Sponsors

The Third Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) in line with the diagnostic criteria of cervical disc herniation: preoperative cervical MRI or CT showed C3-4, C4-5, C5-6, C6-7 or C7-T1 disc herniation, the clinical manifestations of one or both sides Neck and shoulders, upper limb pain or (and) numbness, or gait instability, walking a sense of cotton, etc., imaging and clinical manifestations consistent; (2) cervical MRI confirmed no serious or long-term spinal cord compression caused by spinal degeneration, softening, no intervertebral joint instability; (3) Aged 20 to 90 years old patients with disease duration of 1 to 20 years; (4) after a combination of ineffective conservative treatment or symptoms of recurrent effects of work and life; (5) Pain intensity was evaluated by NRS score scale, and the average intensity of pain was =4 points; (6) no other neurological diseases and mental illness before surgery, heart and lung function was no obvious abnormalities, liver, kidney, electrolyte function was normal, blood sugar, blood pressure control and stability. ASA I-II level, to understand, with the clinical examination and treatment of patients.

Exclusion criteria

Exclusion criteria: (1) does not meet the diagnostic criteria of cervical disc herniation patients; (2) compression of the cervical spinal cord ischemia, softening or severe spinal cord injury patients; (3) cervical disc herniation, prolapse or calcification, nucleus pulposus free patients; (4) patients with cervical spinal stenosis; (5) patients with intervertebral instability or vertebral spondylolisthesis; (6) patients with severe cervical hyperosteogeny; (7) disc calcification or posterior longitudinal ligament calcification in patients; (8) severe cardiopulmonary disease can not tolerate minimally invasive surgery in patients; (9) patients with abnormal coagulation; (10) patients with carotid plaque or carotid sinus sensitivity; (11) patients implanted with pacemakers in vivo; (12) patients with thyroid hyperthyroidism or thyroid nodules; (13) patients with anterior cervical disc anterior surgery; (14) patients with malignant tumors, mental illness and other medical history; (15) Patients who refused to undergo the surgery.

Design outcomes

Primary

MeasureTime frame
pain score;

Secondary

MeasureTime frame
Neurological function score;The overall evaluation of the comprehensive effect;Surgical satisfaction;Once again accept the same surgical intention;Evaluation of the degree of protrusion reduction;The degree of intervertebral disc degeneration;Number of recurrent cases;

Countries

China

Contacts

Public ContactHuang Dong

The Third Xiangya Hospital of Central South University

huangdong6619@vip.163.com+86 13787412741

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026