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The study on the use of neuromuscular blocking agents in daycase surgical children

Efficacy and safety of different doses of mivacurium in daycase urologic surgery for laryngeal mask airway in children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068311
Enrollment
Unknown
Registered
2023-02-14
Start date
2021-03-01
Completion date
Unknown
Last updated
2023-10-30

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

Conditions

urologic surgery

Interventions

Group A:mivacurium (0.15 mg.kg-1)
Group B:mivacurium (0.20 mg.kg-1)
Group C:mivacurium (0.25 mg.kg-1)

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Aged 3–12 years; 2. American Society of Anesthesiologists (ASA) physical status I to II; 3. No abnormalities in laboratory and imaging examinations before operation; 4. Children's family were informed consent.

Exclusion criteria

Exclusion criteria: 1. Respiratory infection, nervous system and cardiovascular diseases, impaired kidney or liver function; 2. Hypersensitivity to mivacurium and other anesthetic agents; 3. Neuromuscular and metabolic diseases; 4. Muscle relaxant administration during the previous 7 days, participation in any clinical subjects within the previous 30 days before the study, children who need to receive antibiotics that effect neuromuscular blocking agents (NMB); 5. Laryngeal mask placement times >= 3 and/or poor placement of laryngeal mask airway; 6. 20% deviation from ideal child body weight.

Design outcomes

Primary

MeasureTime frame
The onset time;duration of clinical action;duration of total action;recovery index;

Secondary

MeasureTime frame
blood pressure;heart rate;SpO2;

Countries

China

Contacts

Public ContactXueping Han

The First Affiliated Hospital of Zhengzhou University

hanxueping66@sina.com+86 13526630125

Outcome results

None listed

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