Skip to content

Remimazolam and propofol in patients with cerebrovascular intervention after surgery Effects of short-term cognitive function and early quality of recovery Research protocol

Remimazolam and propofol in patients with cerebrovascular intervention after surgery Effects of short-term cognitive function and early quality of recovery Research protocol

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110894
Enrollment
Unknown
Registered
2025-10-22
Start date
2025-10-31
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Cerebrovascular disease

Interventions

Propofol group:Anesthesia induced propofol 1.0~1.5 mg/kg, followed by intravenous sufentanil 0.3~0.4 µg/kg and cis-atracurium 0.15 mg/kg, and the anesthesia maintenance group P group was administered
Remimazolam group:Anesthesia was induced with remimazolam 0.3 mg/kg, followed by intravenous sufentanil 0.3~0.4 µg/kg and cis-atracurium 0.15 mg/kg, anesthesia maintenance intravenous infusion of remi

Sponsors

Department of Anesthesiology, The First Affiliated Hospital of the University of Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Gender is not limited 2. Age >= 18 years old 3. Patients who have been clearly diagnosed with cerebrovascular intervention under general anesthesia 4. BMI 18~30kg/m^2; 5. ASA grade II. to III. 6. Mini-cog scale 1-3 points 7. Fully informed consent of the patient.

Exclusion criteria

Exclusion criteria: 1. Subjects who are undergoing other clinical trials 2. Use of opioid analgesics within 24 hours before surgery 3. History of metabolic diseases (metabolic syndrome, diabetes, etc.) 4. History of allergy to the drugs in this study 5. Severe arrhythmias (such as sinus bradycardia, atrioventricular block, etc.) 6. Severe liver and kidney function abnormalities 7. History of severe psychiatric or neurological diseases 8. Mini-cog scale 0 points 9. Other reasons are not suitable for this investigator

Design outcomes

Primary

MeasureTime frame
RAAS score;3D-CAM scoring;Glasgow Rating;Clock test;Postoperative recovery quality assessment scale;

Secondary

MeasureTime frame
Total dosage of Remimazolam;Total amount of propofol used;Total dosage of norepinephrine use;Total usage of remifentanil;HR, BP, and SPO2 values at T1 (upon entering the room), T2 (during intubation), T3 (during surgical puncture), T4 (during surgical embolization/stent placement), T5 (while using the stapler), T6 (upon entering PACU), T7 (during extubation), and T8 (upon leaving PACU);Intraoperative fluid volume;Blood loss;Urine output;Time to response after entering the PACU (calculated from the cessation of study drug infusion);Awake time;Time to recovery of spontaneous breathing;Time of tube removal;PACU stay duration;Adverse event;PACU Medication;

Countries

China

Contacts

Public ContactFang Kang

Department of Anesthesiology, The First Affiliated Hospital of the University of Science and Technology of China

Kangfang199771@163.com+86 181 5512 7799

Outcome results

None listed

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