Trial · NCT04032119
RCT of Gastric ESD With or Without Epineprhine Added Solution
NCT04032119, Phase 3, Completed, Chinese University of Hong Kong
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. RCT of Gastric ESD With or Without Epineprhine Added Solution. Trials, record NCT04032119. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04032119
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- RCT of Gastric ESD With or Without Epineprhine Added Solution
- NCT number
- NCT04032119
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 800 participants, actual
- Lead sponsor
- Chinese University of Hong Kong
- Conditions
- Gastric Neoplasm, Early Gastric Cancer
- Interventions
- Endoscopic submucosal dissection, Epinephrine
- First posted
- 2019-07-25
- Last updated
- 2025-05-04
Source ClinicalTrials.gov
Registered outcomes16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Overall procedural time | During the endoscopic procedure | From the beginning of mucosal incision till the end of submucosal dissection, excluding time for prophylactic homeostasis |
| Secondary | Number of intra-procedural hemorrhage events | During the endoscopic procedure | The number of oozing or spurting bleeding events during a procedure, requiring hemostasis with coagulating forceps |
| Secondary | Maximum systolic blood pressure | During the endoscopic procedure | Maximum systolic blood pressure during ESD |
| Secondary | Maximum heart rate | During the endoscopic procedure | Maximum heart rate during ESD |
| Secondary | Adverse event - Delayed hemorrhage | 30 days | Delayed hemorrhage (Based on CTCAE definition) |
| Secondary | Adverse event - Perforation | 30 days | Perforation (Based on CTCAE definition) |
| Secondary | Adverse event - Cardiovascular event | 30 days | Cardiovascular event (Based on CTCAE definition) |
| Secondary | Adverse event - Cerebrovascular event | 30 days | Cerebrovascular event (Based on CTCAE definition) |
| Secondary | Other adverse event | 30 days | Based on CTCAE definition |
| Secondary | Pathology | During the endoscopic procedure | Final histology based on Vienna Classification |
1 to 10 of 16Source ClinicalTrials.gov
See all 16 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 41620139 | DERIVED |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT04032119
GET https://conductscience.org/api/trials/v1/NCT04032119/registered