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Clinical Trials in South Korea / NCT06984952
Recruiting Not applicable

Effectiveness of ERAS on Postoperative Recovery After Minimally Invasive Gastrectomy

NCT06984952 · tracked via the Priya Life Science South Korea tracker
Phase
Not applicable
Started
2025-06-13
Last updated
2025-09-05

Condition(s) studied

Enhanced Recovery After SurgeryGastrectomy for Gastric Cancer

Investigational drug(s) / intervention(s)

ERAS protocol

ERAS protocol: The ERAS protocol includes pre-admission patient education through audiovisual materials; reduction of perioperative fasting duration with preoperative carbohydrate loading and early postoperative oral intake; multimodal prophylaxis for postoperative nausea and vomiting; early removal of surgical drains and intravenous lines; early mobilization; and multimodal analgesia aimed at minimizing postoperative opioid use. The detailed protocol used in this study has been published previously \[https://doi.org/10.5230/jgc.2025.25.e27\].

Study summary

This prospective, randomized, open-label, multicenter study is designed to evaluate the impact of an enhanced recovery after surgery (ERAS) protocol on the rate of meeting discharge criteria in patients undergoing minimally-invasive gastrectomy for gastric cancer. We hypothesize that implementation of our ERAS protocol will significantly increase the proportion of patients who meet standardized discharge criteria following minimally-invasive gastrectomy.

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults aged ≥19 years scheduled to undergo elective laparoscopic or robotic gastrectomy for gastric cancer * American Society of Anesthesiologists physical status classification I to III * Ability to provide written informed consent, demonstrate understanding of the study protocol, and complete patient-reported outcome measures appropriately Exclusion Criteria: * Requirement for resection of organs other than the stomach during surgery (except for cholecystectomy) * History of upper abdominal surgery (except for cholecystectomy) * Known hypersensitivity to fentanyl, ropivacaine, acetaminophen, or non-steroidal anti-inflammatory drugs * Determined by the investigator or study personnel to be otherwise unsuitable for participation in the study

Primary outcome measure(s)

Trial sites (10)

FacilityCityRegionStatus
Pusan National University Hospital Busan South Korea Not Yet Recruiting
Dongsan Hospital, Keimyung University School of Medicine Daegu South Korea Recruiting
Chungnam National University Hospital Daejeon South Korea Not Yet Recruiting
National Cancer Center Goyang South Korea Not Yet Recruiting
Seoul National University Bundang Hospital Seongnam South Korea Not Yet Recruiting
Seoul National University Hospital Seoul South Korea Recruiting
Seoul St. Mary's Hospital Seoul South Korea Not Yet Recruiting
Severance hospital Seoul South Korea Not Yet Recruiting
SMG-SNU Boramae Medical Center, Seoul South Korea Not Yet Recruiting
Ajou University School of Medicine Suwon South Korea Not Yet Recruiting

More Seoul National University Hospital trials in South Korea

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06984952 on ClinicalTrials.gov ↗ ← All trials in South Korea