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Long-term Follow-up of Bio-signals and Quality of Recovery Following Implementation of Enhanced Recovery After Surgery(ERAS) Program
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
Age
20 - 70 years
Sex
FEMALE
Healthy Volunteers
No
Wonju Severance Christian Hospital
Wŏnju, Gangwon-do, South Korea
Start Date
September 1, 2025
Primary Completion Date
October 1, 2025
Completion Date
October 1, 2026
Last Updated
August 28, 2025
200
ESTIMATED participants
Enhanced Recovery After Surgery
PROCEDURE
Usual Care
PROCEDURE
Lead Sponsor
Wonju Severance Christian Hospital
Collaborators
NCT06430957
NCT07454629
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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