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To observe the effect of stellate ganglion block on postoperative throat pain and intraoperative hemodynamics in patients undergoing spinal surgery

To observe the effect of stellate ganglion block on postoperative throat pain and intraoperative hemodynamics in patients undergoing spinal surgery

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085867
Enrollment
Unknown
Registered
2024-06-20
Start date
2024-06-25
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Postoperative sore throat

Interventions

stellate ganglion block group:In the stellate ganglion block group, patients received stellate ganglion block 20min before surgery.
control group:In the control group, only the routine anesthesia induction.

Sponsors

Department of Anesthesiology, Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) All patients met the spinal surgery indications; (2) American Society of Anesthesiologists physical status ?-?, aged 45-80 yr, BMI 18.5-28kg/m2; (3) The patients agreed to the anesthesia plan and surgical treatment plan used in this study and signed the consent form. (4) No contraindications to anesthesia and stellate ganglion block; (5) Consent to use PCA pump and follow up after operation.

Exclusion criteria

Exclusion criteria: (1) There were surgical contraindications; (2) with heart, brain and kidney serious disease; (3)SGB puncture site infection or systemic infection; (4) those who refused stellate ganglion block or who had mental disorders and were unable to cooperate; (5) long-term alcohol abuse, drug abuse history or preoperative long-term use of analgesics; (6) preoperative throat pain or hoarseness or upper respiratory tract infection within 2 weeks; (7) expected difficulty in tracheal intubation; (8) those with severe malnutrition or obesity; (9) patients with allergy to test drugs.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative sore throat;

Secondary

MeasureTime frame
Quality of post-operative recovery;Vital signs;Surgical situation; Pain score at rest;Postoperative sleep quality;Pain score during cough;Recovery of intestinal function after surgery;Rescue analgesic consumption within 24h after surgery;The incidence of postoperative nausea and vomiting;

Countries

China

Contacts

Public ContactMengxing Jia

Affiliated Hospital of Xuzhou Medical University

xzmu_jiamengxing@126.com+86 158 9523 8016

Outcome results

None listed

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