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Effect of succinylcholine on postoperative sore throat in patients with laryngeal mask general anesthesia

Effect of succinylcholine on postoperative sore throat in patients with laryngeal mask general anesthesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056918
Enrollment
Unknown
Registered
2022-02-22
Start date
2022-09-06
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

postoperative sore throat

Interventions

Intervention group:1.0mg/kg succinine was injected intravenously during induction
Control group:None

Sponsors

West China Second Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. ASA <= II; 2. Age: 18-55 years; 3. BMI: 16-28 kg/m^2; 4. Plan to undergo hysteroscopic surgery under general anesthesia of laryngeal mask; 5. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Mouth opening < 3.0cm; 2. High risk of reflux aspiration (such as pregnancy, satiation, gastroesophageal reflux disease or hiatal hernia); 3. Respiratory complications (such as asthma, chronic obstructive pulmonary disease or recent pneumonia); 4. Invasive ventilation within the last 30 days; 5. Severe mental illness; 6. Congenital cleft lip and palate and other oropharyngeal malformation; 7. Personal or family history of malignant high fever.

Design outcomes

Primary

MeasureTime frame
Sore throat occurred 2 hours after operation;

Secondary

MeasureTime frame
Sore throat occurred 6 hours after operation;Postoperative throat VAS score;First success rate;

Countries

China

Contacts

Public ContactXuemei Lin

West China Second Hospital, Sichuan University

xuemeilin__scu@163.com+86 18180609220

Outcome results

None listed

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