Trial · NCT04513808
Total Intravenous Anesthesia and Recurrence Free Survival
NCT04513808, Phase 3, Recruiting, The Cleveland Clinic
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Total Intravenous Anesthesia and Recurrence Free Survival. Trials, record NCT04513808. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04513808
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Total Intravenous Anesthesia and Recurrence Free Survival
- NCT number
- NCT04513808
- Status
- Recruiting
- Phases
- Phase 3
- Enrollment
- 1,614 participants, estimated
- Lead sponsor
- The Cleveland Clinic
- Conditions
- Esophageal Cancer
- Interventions
- Propofol-based total intravenous anesthesia, Sevoflurane intravenous anesthesia
- First posted
- 2020-08-14
- Last updated
- 2026-09-08
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Recurrence-free survival | 4 years | Patients who did not experience cancer recurrence and/or death. |
| Secondary | ICU duration | From ICU admission until the date of ICU discharge or date of death from any cause, whichever came first, assessed up to 100 months | Postoperative time in ICU during initial admission. |
| Secondary | Hospital duration | Up to 100 months | Postoperative time spent in hospital during initial admission. |
| Secondary | QoR-15 | 2 days | Quality of Recovery 15 score on postoperative day 2. |
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/NCT04513808
GET https://conductscience.org/api/trials/v1/NCT04513808/registered