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Clinical Trials/NCT06729736
NCT06729736
Enrolling By Invitation
Not Applicable

Implementation of the Early Recovery After Surgery (ERAS) Protocol in Colorectal Cancer Patients: a Phase II Multi-Center, Prospective Single Arm Study

Seoul National University Hospital1 site in 1 country500 target enrollmentDecember 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Colorectal Cancer
Sponsor
Seoul National University Hospital
Enrollment
500
Locations
1
Primary Endpoint
Postoperative time to discharge criteria
Status
Enrolling By Invitation
Last Updated
last year

Overview

Brief Summary

The goal of this study is to implement and investigate the efficacy of an Early Recovery After Surgery (ERAS) protocol in South Korean colorectal cancer patients.

The primary outcome will be the postoperative time taken to achieve the 'discharge criteria'.

Secondary outcomes will include adherence, hospital stay, early complications, mortality, pain scores, re-admission and quality of life questionnaire scores.

As a single arm study, all participants will be treated according to an ERAS protocol, which includes components such as early ambulation, minimal fasting, multimodal pain control and omission of- or early removal of invasive catheters.

Detailed Description

This multi-center prospective single arm clinical trial aims to investigate each component and item in the ERAS protocol implemented to perioperative care of colorectal cancer patients. The primary endpoint will be the 'postoperative time to discharge criteria'. Discharge criteria will be defined as meeting all the criteria below: * No fever * Eating more than half of given solid diet * No nausea or vomiting * Gas passing or defecation * Able to walk (more than 1 hour a day) * No sign of surgical site infection * Adequate pain control with oral analgesics such as acetaminophen and NSAIDs * No sign of any other complication Secondary outcomes will include: * adherence of each ERAS item within the protocol * postoperative hospital stay * early postoperative complications (within 30 days of surgery) * postoperative mortality * postoperative pain scores (VAS scores) * re-admission within 30 days of surgery * Quality of Recovery questionnaire * Health-related quality of life questionnaire The specific ERAS protocol to be used in this study has been developed by Seoul National University Hospital, benchmarking the 2018 ERAS® society guidelines for colorectal surgery. The implementation process has been helped and guided by the ERAS® Implementation Program of the Encare team. The ERAS protocol includes: * Pre-admission education, counselling and nutritional support * Pre-induction oral analgesics * Minimal fasting and carbohydrate loading * Omission of nasogastric intubation * Intra-operative abdominal nerve block * Early mobilization * Early oral nutrition and minimal IV fluids * Multimodal opioid sparing analgesia * Postoperative nausea and vomiting prophylaxis * Early removal of urinary catheters This study aims to establish evidence on the factors affecting adherence and efficacy of each ERAS category, to guide a future pivotal RCT that will aim to develop a personalized, risk-stratified ERAS protocol that considers surgical risk and patient factors.

Registry
clinicaltrials.gov
Start Date
December 1, 2024
End Date
December 31, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Above the age of 19 years
  • Pathologic diagnosis of colon cancer or rectal cancer
  • Scheduled for minimally invasive (laparoscopic or robotic) colorectal cancer surgery
  • Agreed to participate after a detailed explanation of the study

Exclusion Criteria

  • Stage 4 (distant metastasis)
  • Emergency surgery
  • Scheduled for transanal surgery
  • Perforated colorectal cancer
  • Obstructed colorectal cancer
  • Familial colorectal cancer (HNPCC, FAP, MUYH polyposis, Peutz-Jeghers syndrome)
  • Previous treatment for colorectal cancer
  • History of other cancer within 5 years (excluding skin cancer)
  • Acute infection
  • Unable to read or understand the study

Outcomes

Primary Outcomes

Postoperative time to discharge criteria

Time Frame: From the date of surgery until the date of first achieving all of the discharge criteria, assessed up to 100 days

The time (days) from initiation of surgery to achieving the discharge criteria. Discharge criteria is defined as meeting all of the following criteria: * No fever * Eating more than half of given solid diet * No nausea or vomiting * Gas passing or defecation * Able to walk (more than 1 hour a day) * No sign of surgical site infection * Adequate pain control with oral analgesics such as acetaminophen and non-steroidal anti-inflammatory drugs (NSAIDs) * No sign of any other complication

Secondary Outcomes

  • Adherence to the ERAS protocol(From date of enrollment to the date of discharge after surgery, assessed up to 100 days)
  • Hospital stay(From the date of hospital admission until the date of discharge after surgery, assessed up to 100 days)
  • Early postoperative complication(From the day of surgery to the 30th postoperative day)
  • Postoperative mortality(From day of surgery until the end of clinical data gathering, assessed upto 100 days.)
  • Postoperative pain score: the Numeric Rating Scale (NRS)(From day of surgery until the end of clinical data gathering, assessed upto 100 days.)
  • Re-admission within 30 days(From randomization until the end of clinical data gathering, assessed upto 100 days.)
  • Health-related Quality of Life(From randomization until the end of clinical data gathering, assessed upto 100 days.)

Study Sites (1)

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