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The effect of Sugammadex Sodium on muscle relaxation recovery in patients after suspension laryngoscopy surgery

The effect of Sugammadex Sodium on muscle relaxation recovery in patients after suspension laryngoscopy surgery

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086028
Enrollment
Unknown
Registered
2024-06-24
Start date
2024-07-02
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

ocal cord polyp

Interventions

Sugammadex group (experimental groups, S1):intravious injection of sugammadex sodium
Sugammadex group (experimental groups, S2):intravious injection of sugammadex sodium(When TOF-COUNT>2)
Neostigmine group (control group, N):intravious injection of neostigmine

Sponsors

Dalian Third People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients scheduled for elective suspension laryngoscope surgery under general anesthesia at the Third People's Hospital of Dalian, Liaoning Province.These patients were aged 18-65 years, BMI 18-28 kg/m^2, and classified as ASA I-II.

Exclusion criteria

Exclusion criteria: Exclusion criteria included patients with significant preoperative respiratory or circulatory dysfunction, liver or kidney function abnormalities, mental disorders and communication barriers, allergies to rocuronium, benzodiazepines, or any component of sugammadex sodium, and those known or suspected to have neuromuscular diseases.

Design outcomes

Primary

MeasureTime frame
Extubation time (min);

Secondary

MeasureTime frame
The incidence of bradycardia;The incidence of excessive secretion;

Countries

China

Contacts

Public ContactGe Qian

Dalian Third People's Hospital

931782466@qq.com+86 186 4090 8169

Outcome results

None listed

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