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Trial · NCT04141631

Transfusion Savings in Heart Surgery: Impact of Individual Strategy by Erythropoietin and Metabolic Adjustment (ScvO2)

NCT04141631, Not applicable, Completed, University Hospital, Montpellier

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Transfusion Savings in Heart Surgery: Impact of Individual Strategy by Erythropoietin and Metabolic Adjustment (ScvO2). Trials, record NCT04141631. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04141631

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Transfusion Savings in Heart Surgery: Impact of Individual Strategy by Erythropoietin and Metabolic Adjustment (ScvO2)
NCT number
NCT04141631
Status
Completed
Phases
Not applicable
Enrollment
128 participants, actual
Lead sponsor
University Hospital, Montpellier
Conditions
Cardiac Surgery, Transfusion, Perioperative Anemia
Interventions
EPO (600UI/Kg, sub-cutaneous) and Ferric Carboxymaltose (FCM) (20 mg/kg in 250 mL of saline solution 0.9% over 15 min)
First posted
2019-10-28
Last updated
2026-06-15

Source ClinicalTrials.gov

Registered outcomes9

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryTransfusion incidence at hospital dischargeup to Day 28Number of patients transfused of blood units
SecondaryICU transfusion incidenceat ICU discharge or up to Day 28Number of blood units transfused during ICU stay
Secondarytotal of blood units transfusedup to day 28number of blood units administered per patient
SecondaryHemoglobin level at surgery discharge and Hemoglobin level at 1 month after discharge from hospitalat surgery discharge (or at Day 28) and at 1 month after discharge from hospitalthe last hemoglobin value at surgery discharge and the hemoglobin value at 1 month after discharge from hospital
SecondaryThe total duration of mechanical ventilationat ICU discharge or up to Day 28The total duration of mechanical ventilation in ICU
Secondarylength of stay in ICUup to day 28numbers of days in ICU
SecondaryLength of hospital stayat day 28Length of stay during hospitalization (Between 1 and 28 day)
SecondaryIncidence of Mortalityat day 28Incidence of 28-day mortality
SecondaryIncidence of postoperative events in ICUat day 28
AKI (KDIGO criteria), Cardiac dysfunction (acute heart failure requiring inotrope or extracorporeal life support (ECLS), arrythmia), vascular dysfunction (norepinephrine support without sepsis), respiratory dysfunction (non invasive ventilation devices, secondary intubation,mechanical ventilation more than 12 hours), septic complications (sepsis/septic shock)

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.

Papers5

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
16836558BACKGROUNDPubMed
23673069BACKGROUNDPubMed
27307162BACKGROUNDPubMed
29029990BACKGROUNDPubMed
39022429RESULTPubMed

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT04141631

GET https://conductscience.org/api/trials/v1/NCT04141631/registered