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Effect of ultrasound-guided thyroid cartilage plane block on postoperative sore throat after double-lumen endotracheal intubation.

Effect of ultrasound-guided thyroid cartilage plane block on postoperative sore throat after double-lumen endotracheal intubation.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097565
Enrollment
Unknown
Registered
2025-02-20
Start date
2025-02-24
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

sore throat

Interventions

Group T:Preoperative ultrasound-guided bilateral thyroid cartilage plane block with 2 ml of 0.25% ropivacaine injected on each side
Group C:blank control,simulated interventions using ultrasound only

Sponsors

Luoyang Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists (ASA) class I - III; age 18 - 65 years; body mass index (BMI) between 18 - 27; and patients undergoing elective thoracoscopic surgery under general anesthesia and requiring one-lung ventilation with double-lumen endotracheal intubation.

Exclusion criteria

Exclusion criteria: Contraindications to regional block; failure of initial intubation; history of psychiatric illness or chronic heavy use of opioid analgesics; comorbid asthma and chronic obstructive pulmonary disease; preoperative history of postoperative sore throat, hoarseness, and cough; preoperative indwelling gastric or nutritional tube; history of acute upper respiratory infection within the week prior to the procedure; history of oral or pharyngeal surgery; anticipated difficult airway; expected duration of the procedure greater than 4 hours; Presence of severe cognitive impairment or verbal communication problems; patients who have participated in another clinical trial within 3 months prior to enrollment, or are currently participating in another clinical trial.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative sore throat 6 hours after extubation;

Secondary

MeasureTime frame
Incidence of postoperative sore throat;Postoperative sore throat severity;mean arterial pressure;heart rate;Duration of intubation;Cormack-Lehane Laryngoscope Exposure Rating;Degree of resistance to double-lumen endotracheal tube insertion;Numeric rating scale for postoperative sore throat;

Countries

China

Contacts

Public ContactJie Hu

Luoyang Central Hospital

hujielyzxyy@163.com+86 137 2162 4858

Outcome results

None listed

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