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The Impact of Ciprofol on the General Anesthesia

The Impact of Ciprofol on the Induction and Maintenance of General Anesthesia in Patients Undergoing Elective Surgery

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400093651
Enrollment
Unknown
Registered
2024-12-10
Start date
2024-12-15
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

General anesthesia

Interventions

CPF:None
PPF:None
C+P:None

Sponsors

The First Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years old; 2. Body mass index (BMI) between 18-30 kg/m^2 3. Plan to undergo elective surgery under general anesthesia; 4. Have the ability to comply with the research protocol, voluntarily participate in the research and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Allergy or history of allergy to the investigational drugs or excipients that may have been used in this study 2. Alcohol or drug abuse within 3 months of perioperative period, general anesthesia within 4 weeks of perioperative period, and sedation/anesthetic treatment within 1 day of screening 3. Patients with severe vision, hearing impairment, mental illness, or who are unable to communicate or refuse to communicate with visitors for other reasons 4. Patients with liver and renal insufficiency 5. The clinical trial was not considered appropriate for other reasons

Design outcomes

Primary

MeasureTime frame
Wake up duration;

Secondary

MeasureTime frame
Sleep duration;Adverse reaction rate;

Countries

China

Contacts

Public ContactWang Zhongxing

The First Affiliated Hospital of Sun Yat-sen University

doctorwzx@126.com+86 136 0004 9116

Outcome results

None listed

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