Efficacy and safety of ciprofol in anesthesia during gynecological day surgery

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100053444

Enrollment

Unknown

Registered

2021-11-21

Start date

2022-01-01

Completion date

Unknown

Last updated

2022-10-04

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

Conditions

None listed

Interventions

experimental group:ciprofol injection 0.2ml/Kg

control group:propofol injection 0.2 mL /Kg

Eligibility

Sex/Gender

Female

Age

18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. 200 patients who underwent hysteroscopy, cervical conization or other gynecological day surgery in our hospital from January 2022 to June 2022; 2. Females aged 18 to 64 years; 3. ASA classification 1-2; 4. Those who signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Those who are allergic to soybeans and related drugs; 2. Pregnant women, lactating women; 3. Those who cannot establish venous access at the wrist; 4. The operation time is less than 10 minutes or more than 45 minutes; 5. Patients with missing intraoperative and follow-up data.

Design outcomes

Primary

Measure	Time frame
Anesthesia induction success rate;Time of loss of consciousness;	—

Secondary

Measure	Time frame
Dosage of narcotic drugs;Time of recovery;Stay in hospital for observation;	—

Countries

China

Contacts

Public ContactJi Fanceng

Weifang people's Hospital

jifanceng@163.com+86 13563698838

Outcome results