Effect of target-controlled infusion of different concentrations of remifentanil combined with propofol on PSI and postoperative recovery of patients undergoing gynecological laparoscopic surgery

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000040130

Enrollment

Unknown

Registered

2020-11-22

Start date

2020-11-30

Completion date

Unknown

Last updated

2021-06-07

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

Conditions

postoperative recovery

Interventions

group one:change the target concentration of remifentanil

group two:change the target concentration of remifentanil

group three:change the target concentration of remifentanil

group four:change the target concentration of remifentanil

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who intend to undergo laparoscopic gynecological general anesthesia; 2. ASA physical status I– II; 3. 18–65 years of age; 4. BMI from 18.5 kg/m^2 to 29 kg/m^2.

Exclusion criteria

Exclusion criteria: 1. Poor compliance, can not cooperate with the surgery; 2. disease or injury affecting the central nervous system; 3. bradycardia or bypotension; 4. recent use of psychoactive or analgesic medication, neurologic disorders; 5. allergy to iodine, alcohol or drug abuse.

Design outcomes

Primary

Measure	Time frame
Patient state index;Bispectral index;	—

Secondary

Measure	Time frame
blood presure;heart rate;	—

Countries

China

Contacts

Public ContactSheng Wang

The First Affiliated Hospital of University of Science and Technology of China

iamsheng2020@ustc.edu.cn+86 19156007726

Outcome results

None listed

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