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The effect of a specific cervical nerve block on postoperative pain following cervical laminoplasty.

The effect of preoperative CCEP block on postoperative 24-hour pain in patients undergoing single-door laminoplasty for cervical spinal canal decompression surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119513
Enrollment
Unknown
Registered
2026-02-28
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Cervical degenerative diseases (cervical spinal stenosis, ossification of the posterior longitudinal ligament, cervical instability, degenerative disc disease, etc.)

Interventions

sham group:NONE
CCEP GROUP:CCEP block

Sponsors

The second affiliated hospital of Zhejiang University school of medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. ASA (American Society of Anesthesiologists) physical status classification I–III; 2. Elective C3-C7 posterior cervical spine surgery (posterior approach unilateral open-door laminoplasty) under general anesthesia. 3. The patient understands and voluntarily signs the informed consent. 4. Age range: 18-75 years old, gender not limited.

Exclusion criteria

Exclusion criteria: 1. Hypersensitivity to the study drug (ropivacaine, lidocaine, or other amide-type local anesthetics) or any of its excipients. 2. Participation in other clinical trials or researcher's judgment of ineligibility. 3. Skin infection/injury/anatomical abnormality at the puncture site or the presence of local anatomical abnormality. 4. Expected postoperative mechanical ventilation =24 hours or planned ICU sedation =24 hours. 5. Pregnancy or breastfeeding. 6. Individuals diagnosed with severe mental illness, currently experiencing an acute episode of anxiety or depression, or unable to cooperate with research assessments. 7. History of drug or alcohol abuse.

Design outcomes

Primary

MeasureTime frame
Cumulative opioid consumption 0-24 hours post-surgery;

Secondary

MeasureTime frame
Pain score;First rescue analgesia time;Postoperative nausea and vomiting;Postoperative recovery quality;sleep quality;

Countries

China

Contacts

Public ContactYi Liu

The Second Affiliated Hospital of Zhejiang University School of Medicine

2517097@zju.edu.cn+86 571 87783777

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026