None listed
Conditions
Interventions
Drug, Procedure/Surgery : This is a randomized controlled trial comparing two anesthesia techniques in women undergoing outpatient gynecologic surgery:
The TCI group received intravenous propofol and
Sponsors
The Catholic University of Korea, St. Vincent's Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Adult women aged 19 to 65 years ASA physical status classification I or II Scheduled to undergo outpatient gynecologic surgery under general anesthesia Able and willing to provide written informed consent
Exclusion criteria
Exclusion criteria: Refusal to participate or inability to provide informed consent History of allergy to sedatives or anesthetics used in the study History of sedative abuse or drug dependence Significant underlying respiratory disease Pregnant or suspected pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time to achieve an Aldrete score =9 in the post-anesthesia care unit (minutes) | — |
Secondary
| Measure | Time frame |
|---|---|
| Time to eye opening (minutes);Length of stay in the post-anesthesia care unit (PACU) (minutes);Patient satisfaction score (0–4 scale);Surgeon satisfaction score (0–2 scale);Incidence of respiratory depression | — |
Countries
Korea, Republic of
Contacts
Public ContactSo Young Kwon
The Catholic University of Korea, St. Vincent's Hospital
Outcome results
None listed