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Completed

NCT Number: NCT04032119

RCT of Gastric ESD With or Without Epineprhine Added Solution

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.

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

The Chinese University of Hong Kong, Hong Kong

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About this study

Endoscopic submucosal dissection (ESD) is an endoscopic technique aiming to achieve en-bloc resection of mucosal neoplastic lesion in the gastrointestinal tract. It is now considered as the standard of treatment for early gastric cancer confined to the mucosa, achieving an excellent overall survival comparable to that of surgical resection.

Important adverse events associated with gastric ESD include hemorrhage (intraoperative or delayed) and perforation. The reported incidence of intraprocedural and delayed hemorrhage of gastric ESD is generally higher than that of esophageal or colorectal ESD5. This is likely due to the rich blood supply of the stomach penetrating from the muscularis to the submucosal layer. Bleeding during ESD would result in difficulty in visualizing the correct plane of dissection from blood clots obscuring view of the endoscope. As a result, prolonged procedural time may be required to achieve hemostasis and obtain adequate view for dissection.

There are currently different options of the solution for submucosal injection during gastric ESD. Epineprhine has often been added into these solutions with the aim of causing vasoconstrictive effect and potentially reduce bleeding during the procedure. The use of epinephrine has been recommended when removing larger pedunculated polyps with endoscopic mucosal resection (EMR)6. However the exact clinical benefit of adding epinephrine during gastric ESD has not been proven in the literature. On the other hand, when larger dose of epinephrine is absorbed systemically it may rarely cause significant tachycardia and generalized vasoconstriction, putting patients at risk of myocardial infarction or cerebrovascular accident.

A retrospective propensity score analysis was previously performed in one of our Japanese center (Presented at JGCA 2019, Shizuoka). After adjustment of important confounding factors including age, sex, tumor location, specimen size, depth of tumor invasion, presence of histological ulcer or scar and operators' experience, the addition of epinephrine into submucosal solution was associated with a significantly shorter procedural time upon multivariate analysis. The mean procedural time was 72±54 minutes versus 93±62 minutes with and without epinephrine respectively. (p<0.001) With the encouraging result from a single center retrospective study, we plan to conduct a prospective multicenter randomized controlled study to confirm the benefit of adding epinephrine into the submucosal solution during gastric ESD.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Selection criteria: Presence of intramucosal neoplastic lesions in the stomach planning for endoscopic submucosal dissection (Vienna Classification Category 3 and 4 lesion)
  • Target subjects receiving sufficient briefing from the attending physician regarding the content of this study and providing informed consent for participation

Exclusion criteria

  • Recurrent / remnant lesion after previous endoscopic resection
  • Lesions arising from surgical anastomotic site, such as gastrojejunostomy / gastroduodenostomy.
  • Marked electrolyte abnormalities
  • Hemostatic or coagulative abnormalities
  • Patient on anti-coagulant agents, including warfarin and other direct oral anti-coagulants (those on antiplatelet can be included)
  • Failure of vital organ (heart, lungs, liver, or kidneys) function
  • Allergic to components of injection solutions: Epinephrine, hyaluronic acid etc
  • Other cases deemed by the examining physician as unsuitable for safe treatment

Treatment and study plan

Endoscopic submucosal dissection

Procedure

Endoscopic submucosal dissection

Epinephrine

Drug

Epinephrine

Primary outcomes

  1. Overall procedural time

    Time frame: During the endoscopic procedure

    From the beginning of mucosal incision till the end of submucosal dissection, excluding time for prophylactic homeostasis

Secondary outcomes

  1. Number of intra-procedural hemorrhage events

    Time frame: During the endoscopic procedure

    The number of oozing or spurting bleeding events during a procedure, requiring hemostasis with coagulating forceps

  2. Maximum systolic blood pressure

    Time frame: During the endoscopic procedure

    Maximum systolic blood pressure during ESD

  3. Maximum heart rate

    Time frame: During the endoscopic procedure

    Maximum heart rate during ESD

  4. Adverse event - Delayed hemorrhage

    Time frame: 30 days

    Delayed hemorrhage (Based on CTCAE definition)

  5. Adverse event - Perforation

    Time frame: 30 days

    Perforation (Based on CTCAE definition)

  6. Adverse event - Cardiovascular event

    Time frame: 30 days

    Cardiovascular event (Based on CTCAE definition)

  7. Adverse event - Cerebrovascular event

    Time frame: 30 days

    Cerebrovascular event (Based on CTCAE definition)

  8. Other adverse event

    Time frame: 30 days

    Based on CTCAE definition

  9. Pathology

    Time frame: During the endoscopic procedure

    Final histology based on Vienna Classification

  10. Size of lesion

    Time frame: During the endoscopic procedure

    Size of lesion

  11. Depth of invasion

    Time frame: During the endoscopic procedure

    Depth of tumor invasion

  12. Vertical margin

    Time frame: During the endoscopic procedure

    Vertical margin involvement

  13. Horizontal margin

    Time frame: During the endoscopic procedure

    Horizontal margin involvement

  14. Differentiation

    Time frame: During the endoscopic procedure

    Degree of differentiation for cancer of stomach

  15. Lymphovascular invasion

    Time frame: During the endoscopic procedure

    Lymphovascular invasion on pathology

Sponsors and collaborators

Lead sponsor

Chinese University of Hong Kong

Other

Collaborators

  • Changi General Hospital
  • Fukuoka University
  • Ishikawa Prefectural Central Hospital
  • JCHO Osaka Hospital
  • Japan Community Healthcare Organization Osaka Hospital
  • Kosin University Gospel Hospital
  • Kyoto 2nd Red Cross Hospital
  • Machida General Hospital
  • Nara City Hospital
  • Osaka International Cancer Institute
  • Sapporo Kinentou hospital
  • Wakayama Red Cross Hospital

Registry information

Official study title

Multicenter Randomized Controlled Trial of Gastric Endoscopic Submucosal Dissection With or Without Epineprhine Added Solution

Important dates

Study start
2020
Primary completion
2022
Study completion
2023
First posted
Jul 25, 2019
Registry last updated
May 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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