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Clinical study on improved strategy of antagonizing residual muscle relaxation of rocuronium in patients under general anesthesia by administration of neostigmine

Clinical study on the optimal dose and timing of neostigmine antagonistic effect on rocuronium

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052809
Enrollment
Unknown
Registered
2021-11-05
Start date
2020-12-01
Completion date
Unknown
Last updated
2022-11-20

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

Conditions

residual neuromuscular blockade, RNMB

Interventions

Group A:Neostigmine 0.04 mg / kg was given when TOFC=0
Group B:Neostigmine 0.06 mg / kg was given when TOFC=0
Group C:Neostigmine 0.04 mg / kg was given when TOFR=0.4
Group D:Neostigmine 0.04 mg / kg was given when TOFR=0.4

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.The range of body mass index (BMI) is 18.5 ~ 25 kg / m2; 2.Aged 18 ~ 65 years; 3.ASA I ~ III; 4.Patients undergoing gastrointestinal surgery under elective Intravenous Inhalation Combined with general anesthesia.

Exclusion criteria

Exclusion criteria: 1. History of allergic diseases, mental illness and alcoholism; 2. Long term use of psychotropic drugs and chronic analgesic drugs; 3. Patients with neuromuscular diseases and using drugs that can affect neuromuscular conduction function; 4. Severe heart, brain, liver, kidney, lung and endocrine diseases (cardiac function above grade II, liver function above child Pugh grade A, renal function above ckd1 stage, moderate and severe pulmonary ventilation dysfunction), electrolyte disorder, anemia (HB < 70g / L) and severe infection; 5. Patients whose muscle relaxation monitoring is affected by trauma, surgical history, hypoplasia and deformity at the muscle relaxation monitoring site; 6. Those who are allergic or contraindicated to the drugs in this study; 7. Participants in other drug clinical studies in the past 30 days.

Design outcomes

Primary

MeasureTime frame
TOFR(train-of-four stimulation ratio);

Countries

China

Contacts

Public ContactSu Min

The First Affiliated Hospital of Chongqing Medical University?

ms89011068@163.com+86 13508302749

Outcome results

None listed

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