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Effect of ultrasound-guided stellate ganglion block on postoperative sore throat and recovery quality after thoracic surgery: a prospective randomized controlled study

Effect of ultrasound-guided stellate ganglion block on postoperative sore throat and recovery quality after thoracic surgery: a prospective randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098901
Enrollment
Unknown
Registered
2025-03-14
Start date
2025-03-20
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Postoperative sore throat

Interventions

Group S :Twenty minutes before anesthesia induction, ultrasound-guided scanning of the stellate ganglion on the surgical side was performed, and a single dose of 0.25% ropivacaine 4ml was administered
Group C:Twenty minutes before anesthesia induction, ultrasound-guided scanning of the stellate ganglion on the surgical side was performed, and a single dose of 0.9% saline 4ml was administered

Sponsors

Beijing Chaoyang Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients scheduled for elective thoracoscopic lobectomy/pulmonary segmentectomy under general anesthesia, with a surgery duration of more than 2 hours, ASA I-III, aged >=18 years, have been fully informed preoperatively and have signed the informed consent.

Exclusion criteria

Exclusion criteria: 1.Failure to sign the informed consent form or permanent cancellation of surgery; 2.Presence of coagulation dysfunction; 3.Possibility of infection at the puncture site or systemic infection; 4.Combined with mental illness and opioid addiction; 5.Suffering from upper respiratory tract infection within 1 week before surgery; 6.History of previous oropharyngeal surgery; 7.Combined with asthma or chronic obstructive pulmonary disease; 8.BMI > 35 or very low body weight (body weight less than 40 kg); 9.Preoperative respiratory insufficiency; 10.Conversion to thoracotomy during surgery; 11.Need to be transferred to the intensive care unit with a tracheal tube after surgery.

Design outcomes

Primary

MeasureTime frame
Postoperative sore throat(POST) ;

Secondary

MeasureTime frame
Postoperative sleep quality score;Postoperative recovery quality score;Postoperative pain score;Postoperative PCA dosage;Postoperative sore throat(POST) ;Postoperative Hoarseness;Postoperative Nausea and Vomiting;Intubation Stress Response;rSO2;

Countries

China

Contacts

Public ContactWu Anshi

Beijing Chaoyang Hospital, Capital Medical University

wuanshi88@163.com+86 135 1101 0883

Outcome results

None listed

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