Trial · NCT04728932
Registered outcomes16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 16 of 16
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time to successful ECMO weaning within the 30 days following randomization | Day 30 | |
| Secondary | Mortality | Day 30, Day 60 | |
| Secondary | Total duration of ECMO support | Between inclusion and Day 30/Day 60 | |
| Secondary | Number of ECMO-free days | Between inclusion and Day 30/Day 60 | |
| Secondary | Duration of ICU stay | Between inclusion and Day 60 | |
| Secondary | Duration of hospitalization stay | Between inclusion and Day 60 | |
| Secondary | Major adverse cardiovascular events | Day 30, Day 60 | defined as death, cardiac transplant, escalation to permanent left ventricular assist device, stroke, dialysis, re-hospitalization for heart failure |
| Secondary | Time to improvement in hemodynamic parameters | Between inclusion and Day 60 | |
| Secondary | Time to hemodynamic stabilization | Between inclusion and Day 60 | |
| Secondary | Days with organ failure asessed by sequential organ failure assessment | Between inclusion and Day 30 | |
| Secondary | Duration of hemodynamic support with catecholamines | Between inclusion and Day 30/Day 60 | |
| Secondary | Number of days alive without hemodynamic support | Between inclusion and Day 30/Day 60 | |
| Secondary | Duration of mechanical ventilation | Between inclusion and Day 30/Day 60 | |
| Secondary | Number of days alive without mechanical ventilation | Between inclusion and Day 30/Day 60 | |
| Secondary | Left ventricular function assessed with echocardiography | Day 30 | |
| Secondary | Incidence of adverse drug reactions | Between inclusion and Day 60 |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
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 list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT04728932/registered