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Study on the ED50 and ED95 of Cipeprofol under combined sufentanil

Study on the ED50 and ED95 of Cipeprofol under combined sufentanil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110957
Enrollment
Unknown
Registered
2025-10-23
Start date
2025-10-24
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

Anesthesia

Interventions

Male group:Sufentanil+Cipepofol
Female group:Sufentanil+Cipepofol

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 65 years; 2. ASA Classification I-III; 3. Patients scheduled for elective surgery under general anesthesia, with plans to send to the recovery room after surgery.

Exclusion criteria

Exclusion criteria: 1.Patients with difficult airways; 2.patients with opioid allergy or abuse; 3.patients with severe hypertension; 4.patients with severe arrhythmias (sinus bradycardia, ventricular rate <50 beats per minute; second-degree or higher atrioventricular block or ventricular block; other arrhythmias with a high risk of sinus arrest, such as sick sinus syndrome (SSS)) ; 5. patients with severe heart failure (NYHA) class III or higher; 6.patients with impaired liver or kidney function; 7.patients with pathological obesity; 8.women who are pregnant, in labor, or breastfeeding; 9.patients whose preoperative mental status cannot be independently or accurately determined; 10. patients with a history of psychotropic drug use.

Design outcomes

Primary

MeasureTime frame
ED50/ED95 when BIS <= 60 after Cipepofol injection combinated with sufentanil ;

Secondary

MeasureTime frame
NIBP, heart rate, SpO2,BIS;The total amount of vasoactive drug usage;Total amount of anesthetic drugs during surgery;The time from anesthesia induction to LOC and BIS <= 60, the time from discontinuation to recovery, the duration of surgery, and the duration of anesthesia;Patient comfort level;

Countries

China

Contacts

Public ContactGuan Xuehai

The First Affiliated Hospital of Guangxi Medical University

guan_xh@aliyun.com+86 185 8769 7310

Outcome results

None listed

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