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
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU Amiens Coordinator of this site? Confirm its status | Amiens | France | Recruiting |
| CHU Dijon Coordinator of this site? Confirm its status | Dijon | France | Recruiting |
| Service d'Anesthésie-Réanimation CCV Hôpital Cardiologique Centre Hospitalier et Universitaire de Lille Coordinator of this site? Confirm its status | Lille | France | Recruiting |
| Centre de Réanimation, Hôpital Salengro, CHU Lille Coordinator of this site? Confirm its status | Lille | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.