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Evaluation of muscle relaxation monitoring effect of the prototype device of phonomyography: exploration based on different muscle relaxants

Evaluation of muscle relaxation monitoring effect of the prototype device of phonomyography: exploration based on different muscle relaxants

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300069824
Enrollment
Unknown
Registered
2023-03-27
Start date
2023-01-19
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Muscle Relaxant Monitoring

Interventions

Index test:the prototype device of phonomyography

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: ·18 years old = age =65 years old ·ASA Physical status ?-? ·18.5=BMI=24.9kg/m2

Exclusion criteria

Exclusion criteria: .A history of neuromuscular disease or relevant family history (e.g., myasthenia gravis) .Abnormal finger movement (e.g., history of hand trauma) .Medications that affect neuromuscular junction function (such as lithium or phenytoin) within 3 months .Allergy to study-related medications .Difficult mask ventilation and difficult intubation are possible .Hepatic and renal insufficiency

Design outcomes

Primary

MeasureTime frame
Muscle relaxant recovery time;Consistence;

Secondary

MeasureTime frame
Onset time of muscle relaxant;Non-depolarizing muscle relaxants very deep muscle release time;Non-depolarizing muscle relaxant deep muscle release time;Time for T1 to recover 25%;Time for T1 to recover 75%;Non-depolarizing muscle relaxer recovery index;adverse event;

Countries

China

Contacts

Public ContactQian Li

West China Hospital, Sichuan University

hxliqian@foxmail.com18980601635

Outcome results

None listed

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