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Clinical Observation of Different Maintenance Doses of Mivacurium in Ambulatory Fundus Surgery

Clinical Observation of Different Maintenance Doses of Mivacurium in Ambulatory Fundus Surgery- A Prospective, Randomized, Controlled, Double-Blind Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052351
Enrollment
Unknown
Registered
2021-10-24
Start date
2021-11-15
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Diabetic retinopathy

Interventions

M1 group:Continuous pumping mivacurium 3µg/(kg · min)
M2 group:Continuous pumping mivacurium 6µg/(kg/min)
M3 group:Continuous pumping mivacurium 9µg/(kg/min)

Sponsors

Beijing Tongren Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients who voluntarily participate in the clinical study, and written informed consent should be obtained; 2.Patients undergoing fundus surgery under general anesthesia in day ward; 3.ASA I~II; 4.The age ranges from 18 to 65; 5.BMI 18.5~28 kg/m2; 6.predicted surgical duration less than 2 hours.

Exclusion criteria

Exclusion criteria: 1. Patients with severe heart, brain, liver, kidney, lung, endocrine diseases, electrolyte imbalance, anemia, and severe infection; 2. Patients with obviously difficult airway; history of chronic allergic diseases; history of mental illness, alcoholism or long-term use of psychotropic drugs and chronic analgesics; 3. Patients with neuromuscular system diseases and taking drugs that can affect neuromuscular conduction function; 4. Patients with trauma, surgical history, hypoplasia, deformity, etc. affecting the detection of muscle relaxation at the monitoring site of muscle relaxation; 5. Allergy to the test drug or other contraindications; pregnant and lactating women; 6. Participated in other clinical studies within the past 30 days.

Design outcomes

Primary

MeasureTime frame
The time between withdrawal of muscle relaxants and recovery of TOFr to 90%;

Secondary

MeasureTime frame
Incidence of TOFr < 70% at extubation;Incidence of TOFr < 90% at extubation;Residence time in PACU;Departure time;Extubation time;dose of Intravenous anesthesia;Postoperative muscle relaxation depth;Adverse reactions;PACU score;

Countries

China

Contacts

Public ContactWang Guyan

Beijing Tongren Hospital, Capital Medical University

guyanwang2006@163.com+86 13910985139

Outcome results

None listed

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