Skip to content

Antagonism of Neostigmine in Continuous Infusion of Mivacurium

Antagonism of Neostigmine in Continuous Infusion of Mivacurium: a Randomised Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07524959
Enrollment
120
Registered
2026-04-13
Start date
2026-05-01
Completion date
2026-07-29
Last updated
2026-04-13

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

Conditions

Neuromuscular Blocking Agents

Keywords

Neuromuscular Monitoring, Mivacurium, Neostigmine, Neuromuscular Blocking Agents

Brief summary

In this study, the antagonism of neostigmine, a cholinesterase inhibitor, on continuous infusion of mivacurium during foot and ankle surgery under general anesthesia was investigated, and the appropriate time point of antagonism was explored.

Detailed description

Mivacurium is currently the shortest-acting benzylisoquinoline nondepolarizing muscular relaxant in clinical practice, which is suitable for short surgery. Its continuous infusion can also be used in medium-term surgery with uncertain operation time, which can accelerate the recovery of postoperative muscle relaxation. Whether continuous infusion of mivacurium requires antagonism and the appropriate time point of antagonism is controversial.

Interventions

DRUGNeostigmine

Administer neostigmine at a dose of 0.04 mg/kg (combined with 0.02 mg/kg atropine)

Sponsors

Beijing Tongren Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* 18 - 65 years old; * American Society of Anesthesiologists (ASA) physical stastus classification system: I-II; * Body mass index (BMI) 18.5 - 30 kg/m2 * Patients with normal cholinesterase levels before the operation

Exclusion criteria

* Refusal to participate in the study; * ASA classification of grade III or above; * Severe organ dysfunction, difficult airway or neurological muscle disorders; * Taking drugs that affect neuromuscular monitoring or neuromuscular conduction function; * Allergic to the test drug or having other contraindications; * Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
The time from count 2 to TOFr recovery to 0.9Perioperative

Secondary

MeasureTime frame
The time from count 2 to TOFr recovery to 0.7Perioperative
The time from count 2 to TOFr recovery to 0.4Perioperative
Mean Arterial PressurePerioperative
Blood pressurePerioperative
Heart ratePerioperative
Surgical durationThe start time and end time of the surgery

Countries

China

Contacts

CONTACTHaiyao Wu
haiyaowu0105@163.com0086 18171485811
STUDY_DIRECTORGuyan Wang

Beijing Tongren Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 14, 2026