Trial · NCT06563063
Finding ED90 of Flumazenil for Selective Improvement of Respiratory Distress by Remimazolam
NCT06563063, Not applicable, Completed, Yonsei University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Finding ED90 of Flumazenil for Selective Improvement of Respiratory Distress by Remimazolam. Trials, record NCT06563063. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06563063
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Finding ED90 of Flumazenil for Selective Improvement of Respiratory Distress by Remimazolam
- NCT number
- NCT06563063
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 60 participants, actual
- Lead sponsor
- Yonsei University
- Conditions
- Stomach Neoplasm
- Interventions
- Flumazenil
- First posted
- 2024-08-20
- Last updated
- 2024-08-20
Source ClinicalTrials.gov
Registered outcomes1
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Whether it was successful or unsuccessful to improve the patient's respiratory distress | 30 seconds after the intervention | Respiratory distress occurring during the procedure were defined as follows: 1) sustained hypoxia (SpO2 \< 94%); or 2) excessive irregular breathing with heavy chest and abdominal movement, making it impossible for the endoscopist to perform the procedure. Improvement in respiratory distress was defined as recovery of hypoxia (SpO2 ≥ 95%) and improvement in respiratory pattern-loss of excessively irregular breathing and subdued chest and abdominal movement-within 30 seconds after flumazenil administration to the extent that the procedure could be resumed. |
Source ClinicalTrials.gov
Outcomes0
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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/NCT06563063
GET https://conductscience.org/api/trials/v1/NCT06563063/registered