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NCT05699005RecruitingPhase 1

Individualized or Conventional Transfusion Strategies During Peripheral VA-ECMO

Comparison of an Individualized Transfusion Strategy to a Conventional Strategy in Patients Undergoing Peripheral Veno-arterial ECMO for Refractory Cardiogenic Shock: a Randomized Controlled Trial - ICONE

Source: ClinicalTrials.gov · Last updated 17 Sept 2026

Brief summary (registry, in English)

This multicenter randomized controlled trial compare two transfusion strategies of red blood cells transfusion in patients supported by veno-arterial extracorporeal membrane oxygenation for refractory cardiogenic shock. An individualized transfusion strategy based on ScVO2 level, is compared to a conventionnal strategy based on predefined hemoglobin threshold. The primary endpoint is the consumption of packed red blod cells, secondary endpoints are subgroup analysis, mortality, morbidity, and cost-effectiveness

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
236 (estimated)
First submitted
21 Dec 2022
Start date
18 Sept 2023
Primary completion date
18 Mar 2028
Lead sponsor
University Hospital, Lille
NCT number
NCT05699005

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 236
  • From 18 Sept 2023 to the primary completion date, 18 Mar 2028
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Lab values

  • Known congenital hemoglobin disease or disorder,

Other

  • Pregnancy,
  • Lack of health insurance,
  • Opposition to blood transfusion,
  • Metabolic alcaloosis with pH\>7.8,
  • eCPR,
  • Legally incapacitated adults

Who the study is looking for

  • Age of 18 and older,
  • supported by peripheral VA-ECMO
  • for cardiogenic shock
  • Life expentency \>90 days
  • Central venous line available ScVO2 measurement

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU Amiens
Coordinator of this site? Confirm its status
AmiensFranceRecruiting
CHU Dijon
Coordinator of this site? Confirm its status
DijonFranceRecruiting
Service d'Anesthésie-Réanimation CCV Hôpital Cardiologique Centre Hospitalier et Universitaire de Lille
Coordinator of this site? Confirm its status
LilleFranceRecruiting
Centre de Réanimation, Hôpital Salengro, CHU Lille
Coordinator of this site? Confirm its status
LilleFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.