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Ultrasound-guided superficial cervical plexus combined with deep cervical plexus block in the perioperative analgesic effect of anterior cervical surgery

Ultrasound-guided superficial cervical plexus combined with deep cervical plexus block in the perioperative analgesic effect of anterior cervical surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102766
Enrollment
Unknown
Registered
2025-05-20
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Perioperative pain

Interventions

Control group:only general anaesthesia
Experimental group(CPB group):Incision lateral neck superficial plexus combined with bilateral deep cervical plexus block and general anaesthesia

Sponsors

Second Xiangya Hospital of CSU
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age > 18 years old; 2.Elective posterior cervical surgery; 3.ASA II-III; 4.First cervical spine surgery; 5.Voluntarily sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Contraindications to nerve block: anatomical variations caused by infection, tumor, and severe deformity at the puncture site; coagulopathy; local anesthetics, allergies, etc. 2.history of chronic pain or opioid misuse; 3.mental illness; 4.Use of analgesics before surgery; 5.Liver and kidney dysfunction; 6.Others unsuitable for clinical trial participants;

Design outcomes

Primary

MeasureTime frame
Intraoperative sufentanil dosage;—

Secondary

MeasureTime frame
Postoperative pain;Post-operative recovery situation;—

Countries

China

Contacts

Public ContactXu Junmei

Second Xiangya Hospital of CSU

13975148864@139.com+86 731 85292476

Outcome results

None listed

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