The effects of ciprofol on preoperative anxiety in gynecological patients and the related EEG mechanism research

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2500100973

Enrollment

Unknown

Registered

2025-04-17

Start date

2025-04-21

Completion date

Unknown

Last updated

2025-04-21

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

Conditions

anxiety

Interventions

L-anxiety group:no

H-anxiety group:no

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Female patients older than 18 years old, scheduled for general anesthesia surgery, and willing to participate

Exclusion criteria

Exclusion criteria: History of mental illness and congenital diseases; taking anti-anxiety or anti-depressant drugs; participation in other clinical trials at the same time; refusal to participate.

Design outcomes

Primary

Measure	Time frame
Dosage of propofol or ciprofol in anesthesia induction;	—

Secondary

Measure	Time frame
Power Spectral Density of Electroencephalogram (a,ß,d and ?);	—

Countries

China

Contacts

Public ContactJiaojiao Yang

Zhongda Hospital Southeast University

jollyyang1989@126.com+86 189 1291 8727

Outcome results

None listed

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