RCT of Gastric ESD With or Without Epineprhine Added Solution

NCT04032119 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 800

Last updated 2025-05-04

No results posted yet for this study

Summary

This is an international multi-center randomised controlled study comparing outcomes of gastric endoscopic submucosal dissection (ESD) with or without addition of epinephrine in the submucosal injection solution.

Conditions

  • Gastric Neoplasm
  • Early Gastric Cancer

Interventions

PROCEDURE

Endoscopic submucosal dissection

Endoscopic submucosal dissection

DRUG

Epinephrine

Epinephrine

Sponsors & Collaborators

  • Osaka International Cancer Institute

    collaborator UNKNOWN
  • Fukuoka University

    collaborator OTHER
  • Changi General Hospital

    collaborator OTHER
  • Kyoto 2nd Red Cross Hospital

    collaborator UNKNOWN
  • Ishikawa Prefectural Central Hospital

    collaborator UNKNOWN
  • Kosin University Gospel Hospital

    collaborator OTHER
  • Machida General Hospital

    collaborator UNKNOWN
  • Nara City Hospital

    collaborator UNKNOWN
  • Wakayama Red Cross Hospital

    collaborator UNKNOWN
  • JCHO Osaka Hospital

    collaborator UNKNOWN
  • Sapporo Kinentou hospital

    collaborator UNKNOWN
  • Japan Community Healthcare Organization Osaka Hospital

    collaborator UNKNOWN
  • Chinese University of Hong Kong

    lead OTHER

Principal Investigators

  • Hon Chi Yip, MBChB, FRCSEd · Chinese University of Hong Kong

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-01-10
Primary Completion
2022-12-31
Completion
2023-01-31

Countries

  • Hong Kong
  • Japan
  • Singapore
  • South Korea

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04032119 on ClinicalTrials.gov