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NCT Number: NCT07524959

Antagonism of Neostigmine in Continuous Infusion of Mivacurium

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Beijing tongren Hospital, Capital Medical University

Beijing, Beijing Municipality, 100000, China

Location contact

Haiyaao Wu

CONTACT

[email protected]

008618171485811

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Neostigmine

Drug

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

Primary outcomes

  1. The time from count 2 to TOFr recovery to 0.9

    Time frame: Perioperative

Secondary outcomes

  1. The time from count 2 to TOFr recovery to 0.7

    Time frame: Perioperative

  2. The time from count 2 to TOFr recovery to 0.4

    Time frame: Perioperative

  3. Mean Arterial Pressure

    Time frame: Perioperative

  4. Blood pressure

    Time frame: Perioperative

  5. Heart rate

    Time frame: Perioperative

  6. Surgical duration

    Time frame: The start time and end time of the surgery

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Beijing Tongren Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 13, 2026
Registry last updated
Apr 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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