Effective dose of ciprofol inhibiting responses to artificial airway insertion in different genders

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200061309

Enrollment

Unknown

Registered

2022-06-20

Start date

2022-07-01

Completion date

Unknown

Last updated

2023-04-03

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

Conditions

Drug dosage of ciprofol during induction of anesthesia

Interventions

male group vs female group:Adjust the drug dose according to the response to tracheal intubation

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. ASA I-II; 2. BMI 18.5-28kg/m^2; 3. Patients aged between 18 and 65 years.

Exclusion criteria

Exclusion criteria: 1. Past history of allergy to propofol,egg,peas and beans; 2. Past history of mental illness; 3. Preoperative SBP>=180mmHg, DBP>=110mmHg; 4. Preoperative history of tachycardia or HR>=110 beats/min; 5. Predictably difficult airway.

Design outcomes

Primary

Measure	Time frame
blood pressure;heart rate;Intubation reaction;ED50;ED95;	—

Countries

China

Contacts

Public ContactWei Zhang

chalou666666@126.com+86 13838390767

Outcome results

None listed

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