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The Application Value of Continuous Mivacurium Infusion in Nerve Monitoring During Thyroid Surgery: A Single-Center, Prospective, Randomized Controlled Study

The Application Value of Continuous Mivacurium Infusion in Nerve Monitoring During Thyroid Surgery: A Single-Center, Prospective, Randomized Controlled Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125643
Enrollment
Unknown
Registered
2026-05-29
Start date
2026-05-29
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Thyroid cancer

Interventions

Control group:Mivacurium continuous infusion is not used during the maintenance phase of anesthesia
Experimental group:Continuous infusion of mivacurium was used during the maintenance phase of anesthesia

Sponsors

Shenshan Medical Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged 18 to 65 years, ASA I-II, undergoing elective thyroid surgery; 2.Intraoperative neurophysiological monitoring was used; 3.No history of severe allergy to mikukloramine or other foods and drugs, or allergic diseases; 4.The patient voluntarily participates and has signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Body mass index (BMI) 30 kg/m^2; 2.SBP > 180 mmHg or DBP > 110 mmHg; 3.Those with a history of asthma or other severe allergic conditions; 4.Those with neuromuscular junction diseases such as Parkinson's and myasthenia gravis; 5.Known or suspected atypical plasma cholinesterase gene homozygotes and decreased plasma cholinesterase; 6.Pregnant and breastfeeding women; 7.The patient is generally in poor condition, with a medical history of severe cardiovascular, respiratory, liver and kidney, central nervous system, and hematological diseases. 8.People who abuse alcohol or rely on painkillers or psychiatric medications; 9.Concurrent use of contraindicated drugs

Design outcomes

Primary

MeasureTime frame
Satisfaction with the surgery;Conditions for tracheal intubation;Depth of anesthesia;

Secondary

MeasureTime frame
Adverse reaction;Awakening-related indicators;

Countries

China

Contacts

Public ContactLiu Ling

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

liuling23@mail.sysu.edu.cn+86 20 8133 2060

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026