The ECMOCYP (cytochromes P450 Activity) Study

RecruitingOBSERVATIONAL
Enrollment

46

Participants

Timeline

Start Date

October 31, 2024

Primary Completion Date

July 31, 2026

Study Completion Date

July 31, 2026

Conditions
ECMOCardiogenic ShockTemporary Mechanical Circulatory Support
Interventions
DIAGNOSTIC_TEST

phenotype

"Eligible patients will receive orally the cocktail probe drugs ( via a naso-gastric tube at D3 after tMCS implantation or after the beginning of the cardiogenic shock for the control group) and via an oral administration at 14 days after tMCS explantation (or cardiogenic shock termination for the control group defined as: no need to use inortropic or vasopressive agent and absence of organ insufficiency). The phenotyping probe drugs of the Geneva Cocktail will be given as: one capsule containing the remaining probe 'cocktail' drugs. According to clinical experience in our intensive care unit department, inflammation related to tMCS peaks at D3 after tMCS implantation.~Blood samples will be collected from the central venous line 2 hours after drug administration for CYP phenotyping and genotyping. Inflammatory markers blood levels (Il-6, TNF-α, Il-1β, IFN-γ) will be measured at tMCS implantation or shock initiation and at the same time than CYP phenotyping."

Trial Locations (1)

1205

RECRUITING

University Hospital Of Geneva, Geneva

All Listed Sponsors
collaborator

Jean Terrier

UNKNOWN

collaborator

Benjamin Assouline

UNKNOWN

collaborator

Raphël Giraud

UNKNOWN

collaborator

Karim Bendjelid

UNKNOWN

collaborator

Caroline Samer

UNKNOWN

collaborator

Youssef Daali

UNKNOWN

collaborator

Anastasia Zaslavskaya

UNKNOWN

lead

University Hospital, Geneva

OTHER