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Effect of ciprofol combined with remifentanil anesthesia on the intraoperative neuroelectrophysiological monitoring in microvascular decompression of facial nerve

Effect of ciprofol combined with remifentanil anesthesia on the intraoperative neuroelectrophysiological monitoring in microvascular decompression of facial nerve

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063638
Enrollment
Unknown
Registered
2022-09-13
Start date
2022-09-05
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

Facial spasm

Interventions

ciprofol group:Anesthesia and sedation were induced and maintained with cyclopofol.
propofol group:Anesthesia and sedation were induced and maintained with propofol

Sponsors

The First Affiliated Hospital of University of Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Unilateral disease, the first operation for hemifacial spasm; 2. Abnormal EMG response and facial nerve motor evoked potential were monitored by electrophysiological monitoring technique during operation; 3. Patients aged 18-70 years; 4. ASA classification II-III.

Exclusion criteria

Exclusion criteria: 1. Patients with secondary hemifacial spasm; 2. Patients with neuromuscular dysfunction; 3. Allergic to cyclopofol, propofol and other anesthetic drugs; 4. Abnormal liver and kidney function; 5. Long-term use of sedative and hypnotic drugs; 6. BMI over 30.

Design outcomes

Primary

MeasureTime frame
Amplitude changes of facial nerve motor evoked potentials during operation;

Secondary

MeasureTime frame
Success of intraoperative abnormal EMG response monitoring;Heart rate, mean arterial pressure, BIS value, cardiac function related indexes;Anesthesia time, operation time, recovery time, extubation time, anesthetic drug dosage;Intubation reaction, injection pain during induction period;Intraoperative unexpected body movement, spontaneous breathing recovery, intraoperative awareness;Restlessness, nausea and vomiting during the recovery period;Surgical outcomes and neurological complications;

Countries

China

Contacts

Public ContactLi Juan

The First Affiliated Hospital of University of Science and Technology of China

huamuzi1999@126.com+86 181 5512 3312

Outcome results

None listed

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