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Comparison of ciprofol versus propofol for Anesthesia during gynecological day surgery:A prospective, randomized, double-blind, non-inferiority trial

Comparison of ciprofol versus propofol for Anesthesia during gynecological day surgery:A prospective, randomized, double-blind, non-inferiority trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080000
Enrollment
Unknown
Registered
2024-01-18
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

None

Interventions

Sponsors

Weifang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who plan to undergo gynecological hysteroscopic daytime surgery under general anesthesia; 2. The American Association of Anesthesiologists (ASA) grade I-II; 3. Aged between 18 and 65 years old; 4. 18.5=BMI<28

Exclusion criteria

Exclusion criteria: Patients who are allergic to experimental drugs

Design outcomes

Primary

MeasureTime frame
The success rate of anesthesia;

Secondary

MeasureTime frame
Duration of successful anesthesia induction;The duration of patient's awakening from anesthesia;Vital signs of patients at multiple time points during anesthesia;Additional dosage and frequency of medication required during anesthesia;Patient satisfaction;

Countries

China

Contacts

Public ContactJi Fanceng

Weifang People's Hospital

hunter-1986@163.com+86 135 6369 8838

Outcome results

None listed

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