Trial · NCT01938079
Pharmacokinetic Alterations During ECMO
NCT01938079, Not applicable, Completed, Columbia University; results first posted 2016-09-29
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Pharmacokinetic Alterations During ECMO. Trials, record NCT01938079. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01938079
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Pharmacokinetic Alterations During ECMO
- NCT number
- NCT01938079
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 20 participants, actual
- Lead sponsor
- Columbia University
- Conditions
- Acute Respiratory Failure
- Interventions
- Ketamine, Sedative drug regimen
- First posted
- 2013-09-10
- Last updated
- 2016-09-29
- Results first posted
- 2016-09-29
Source ClinicalTrials.gov
Registered outcomes1
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Cumulative Fentanyl Equivalents From ECMO Initiation to Decision to Achieve Wakefulness | Up to 14 days | Culmulative fentanyl equivalents meaning the combination of sedative drug regimen - measured in mg - from ECMO initiation to decision to achieve wakefulness. |
Source ClinicalTrials.gov
Outcomes1
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Cumulative Fentanyl Equivalents From ECMO Initiation to Decision to Achieve Wakefulness | Up to 14 days | mg | MEDIAN |
Source ClinicalTrials.gov
Results by group2
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Cumulative Fentanyl Equivalents From ECMO Initiation to Decision to Achieve Wakefulness | Sedative Without Ketamine | 330 | Inter-Quartile Range 101 to 1971 | mg | |
| Cumulative Fentanyl Equivalents From ECMO Initiation to Decision to Achieve Wakefulness | Sedative With Ketamine | 834 | Inter-Quartile Range 379 to 2329 | mg |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Sedative Without Ketamine | 10 | |
| Overall Study | STARTED | Sedative With Ketamine | 10 | |
| Overall Study | COMPLETED | Sedative Without Ketamine | 10 | |
| Overall Study | COMPLETED | Sedative With Ketamine | 10 | |
| Overall Study | NOT COMPLETED | Sedative Without Ketamine | 0 | |
| Overall Study | NOT COMPLETED | Sedative With Ketamine | 0 |
Source ClinicalTrials.gov
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 totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Sedative Without Ketamine | ||
| Total, all-cause mortality | Sedative With Ketamine | ||
| Total, other adverse events | Sedative Without Ketamine | 0 | 10 |
| Total, other adverse events | Sedative With Ketamine | 0 | 10 |
| Total, serious adverse events | Sedative Without Ketamine | 0 | 10 |
| Total, serious adverse events | Sedative With Ketamine | 0 | 10 |
Source ClinicalTrials.gov
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 comparisons1
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison |
|---|
| Sedative Without Ketamine vs Sedative With Ketamine: serious adverse events |
Source Trial comparisons
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/NCT01938079
GET https://conductscience.org/api/trials/v1/NCT01938079/registered