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Effect of ultrasound-guided middle cervical plexus block versus superficial cervical plexus block on quality of recovery after anterior cervical approach surgery: a prospective, double-blind, randomized controlled trial

Effect of ultrasound-guided middle cervical plexus block versus superficial cervical plexus block on quality of recovery after anterior cervical approach surgery: a prospective, double-blind, randomized controlled trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072280
Enrollment
Unknown
Registered
2023-06-08
Start date
2023-06-10
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 spondylosis

Interventions

ICPB group:intermediate cervical plexus block, ICPB
SCPB group:superficial cervical plexus block

Sponsors

Ganzhou People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Planned anterior cervical spine surgery; 2. ASA 1-2; 3. Aged 18-75 years.

Exclusion criteria

Exclusion criteria: 1. Any contraindication to regional anesthesia (e.g. local infection, coagulation disorders); 2. Known hypersensitivity to local anesthetics, mental disorders, and drug or alcohol abuse; 3. Cognitive dysfunction; 4. Emergency surgery patients; 5. Patients with severe respiratory disease; 6. Patients or surgeons refuse.

Design outcomes

Primary

MeasureTime frame
QoR-15;—

Secondary

MeasureTime frame
NRS score at rest and during movement 24h after operation;Intraoperative remifentanil dosage;Time to first rescue analgesia;Postoperative analgesic use;Adverse Events;Nausea, vomiting;Length of stay;—

Countries

china

Contacts

Public ContactRuipeng Zhong

Ganzhou People's Hospital

530539437@qq.com+86 150 7975 0272

Outcome results

None listed

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