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Application of sugammadex sodium in the recovery period of general anesthesia in patients with uvulopalatopharyngoplasty

Application of sugammadex sodium in the recovery period of general anesthesia in patients with uvulopalatopharyngoplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100996
Enrollment
Unknown
Registered
2025-04-17
Start date
2025-05-06
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Obstructive Sleep Apnea-Hypopnea Syndrome

Interventions

Sugammadex group (Group S):After the operation, the infusion of general anesthetics was stopped, and when T2 of TOF reappeared, group S was injected Sugammadex with 5ml of (2mg/kg) saline diluent wit
Neostigmine Formation (Group N):After surgery, the infusion of general anesthetics was stopped, and when T2 of TOF reappeared, group N was injected 5ml of neosmin (0.02mg/kg) and atropine (0.01mg/kg)

Sponsors

The Second Norman Bethune Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.All enrolled patients underwent UPPP surgery, and the preoperative examination and evaluation met the indications. 2.Patients and their families should give informed consent to the study, sign informed consent forms, and the medical ethics Committee should approve the study. 3.No contraindications to anesthesia, no serious cardiopulmonary and other important organ dysfunction or serious systemic diseases. 4.American Society of Anesthesiologists grade I to II.

Exclusion criteria

Exclusion criteria: 1.Patients with mental disorders, psychological disorders or loss of consciousness. 2.Patients with surgical contraindications. 3.Intolerance or history of allergy to narcotic drugs. 4.Patients with diseases of the blood system or immune system. 5.Patients with myasthenia gravis. 6.Patients with abnormal heart, liver and kidney function.

Design outcomes

Primary

MeasureTime frame
The 24-h postoperative Quality of Recovery-15 (QoR-15) score;

Secondary

MeasureTime frame
Neuromuscular recovery time (time to recovery of a train-of-four (TOF) ratio =0.9);Extubation time ;Diaphragmatic excursion ;:Postoperative complications ;Intraoperative outcomes ;Post-anesthesia care unit (PACU) outcomes;

Countries

China

Contacts

Public ContactZhao Peng

The Second Norman Bethune Hospital of Jilin University

zhaopeng8933@126.com+86 135 0430 8933

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026