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Clinical study of residual NMB after general anesthesia using grip strength evaluation

Clinical study of residual NMB after general anesthesia using grip strength evaluation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17011208
Enrollment
Unknown
Registered
2017-04-21
Start date
2017-04-25
Completion date
Unknown
Last updated
2017-04-24

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

Conditions

Clinical studies in patients after general anesthesia residual NMB

Interventions

1:cisatracurium
2:rocuronium

Sponsors

Jiaxing Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 70 Years

Inclusion criteria

Inclusion criteria: Selective laparoscopic cholecystectomy in patients, aged 19 to 70 years, ASA ?-II level.

Exclusion criteria

Exclusion criteria: 1. combined with neuromuscular disease; 2. severe cardiovascular disease; 3. severe lung disease; 4. severe liver and kidney disease; 5. deaf patients; 6. hand or upper limb disability patients.

Design outcomes

Primary

MeasureTime frame
Rate of the TOFr equal to 0.7;Rate of the TOFr equal to 0.8;Rate of the TOFr equal to 0.9;Rate of the TOFr equal to 0.25 after 60 minutes;Time of TOFr shift from 0.25 to 0.75;Time of TOFr shift from 0.25 to 0.9;—

Countries

China

Contacts

Public ContactZhou Qinghe

Jiaxing Second Hospital Department of Anesthesiology

jxxmxy@163.com+86 13732573379

Outcome results

None listed

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