The goal of this clinical trial is to evaluate the effect of an Enhanced Recovery After Surgery(ERAS) protocol in patients undergoing gynecologic laparoscopic surgery under general anesthesia. The main question it aims to answer is: Does the ERAS protocol improve the quality of recovery compared to standard treatments? Researchers will compare ERAS protocol with standard treatment to see if ERAS protocol improves the quality of recovery after surgery. Participants will: * Receive ERAS protocol during the hospitalization * Undergo bio-signal monitoring for one month using Hi-Cardi Plus device and Galaxy Watch 7 * Visit the hospital at one week and one month after discharge * Complete questionnaires(QOR-15K, WHO-DAS 2.0, EQ-5D-3L) at 24 hours after surgery, at discharge, one week after discharge, and one month after discharge
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Quality of Recovey-15, Korean version (QoR-15K)
Timeframe: on 24 hours postoperatively
Quality of Recovey-15, Korean version (QoR-15K)
Timeframe: one week after hospital discharge
Quality of Recovey-15, Korean version (QoR-15K)
Timeframe: one month after hospital discharge
The World Health Organization Disability Assessment Schedule, 2nd Edition (WHODAS 2.0)
Timeframe: on 24 hours postoperatively
The World Health Organization Disability Assessment Schedule, 2nd Edition (WHODAS 2.0)
Timeframe: one week after hospital discharge
The World Health Organization Disability Assessment Schedule, 2nd Edition (WHODAS 2.0)
Timeframe: one month after hospital discharge
EuroQol 5-Dimension, 3-Level questionnaire (EQ-5D-3L)
Timeframe: on 24 hours postoperatively
EuroQol 5-Dimension, 3-Level questionnaire (EQ-5D-3L)
Timeframe: 1 week after hospital discharge
EuroQol 5-Dimension, 3-Level questionnaire (EQ-5D-3L)
Timeframe: 1 month after hospital discharge