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NCT07345559Recruiting

Personalisation of Mean Arterial Pressure in Adult Patients With Cardiogenic Shock

Prospective, Randomized, Multicenter, Controlled Trial Assessing the Personalization of Mean Arterial Pressure in Adult Patients With Cardiogenic Shock

Source: ClinicalTrials.gov · Last updated 29 Sept 2026

Brief summary (registry, in English)

Cardiogenic shock is a life-threatening condition characterized by inadequate cardiac output, leading to organ hypoperfusion and high mortality. Maintaining mean arterial pressure (MAP) is crucial, but standard targets may be insufficient due to venous congestion. Central venous pressure (CVP) can help assess effective perfusion pressure. This study investigates whether a personalized MAP target adjusted by CVP improves organ function and survival compared to standard MAP management.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
406 (estimated)
First submitted
27 Nov 2025
Start date
26 Mar 2026
Primary completion date
25 Jul 2029
Lead sponsor
CMC Ambroise Paré
NCT number
NCT07345559

What you commit to

  • Study type: Interventional
  • Planned participants: 406
  • From 26 Mar 2026 to the primary completion date, 25 Jul 2029
  • 11 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.

Prior treatment

  • Chronic dialysis or presence of renal replacement therapy criteria at inclusion ;
  • Recovered cardiopulmonary arrest within 7 days prior to inclusion;

Lab values

  • Chronic kidney disease stage G4 (defined by an eGFR between 15-29 ml/min/1.73 m²) or G5 (defined by an eGFR less than 15 ml/min/1.73 m²) according to the KDIGO CKD classification at inclusion;
  • Hypersensitivity to norepinephrine tartrate or to any of the following excipients: sodium chloride, hydrochloric acid or sodium hydroxide water for injectable preparations;

Other

  • Catecholamine infusion for more than 24 consecutive hours;
  • CVP \< 5 mm Hg at inclusion;
  • MAP \> 70 mmHg at inclusion;
  • Patient already on mechanical circulatory support at inclusion before enrollment (patients who receive support after inclusion will not be excluded);
  • Primary diagnosis of tamponade, pulmonary embolism, or septic shock;
  • Absence of central venous access;
  • Known pregnancy or current breastfeeding;
  • Under legal guardianship, curatorship, or judicial protection.

Who the study is looking for

  • Aged ≥18 years
  • Cardiogenic shock state, according to the consensus definition,
  • SCAI (Society for Cardiovascular Angiography and Interventions) classification ≥ C
  • Consent from the patient or close relative / trusted person or emergency inclusion procedure
  • Benefiting fromciary of a social security scheme

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

Full criteria on ClinicalTrials.gov

Sites (11)

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

SiteCityCountrySite status
CHU d'Amiens-Picardie
Coordinator of this site? Confirm its status
AmiensFranceNot yet recruiting
Hopital Henri Mondor
Coordinator of this site? Confirm its status
CréteilFranceRecruiting
Hôpital Privé Jacques Cartier
Coordinator of this site? Confirm its status
MassyFranceNot yet recruiting
CMC Ambroise Paré Hartmann
Coordinator of this site? Confirm its status
Neuilly-sur-SeineFranceRecruiting
CHU d'Orléans
Coordinator of this site? Confirm its status
OrléansFranceNot yet recruiting
Hôpital Lariboisière
Coordinator of this site? Confirm its status
ParisFranceNot yet recruiting
Hôpital Cochin
Coordinator of this site? Confirm its status
ParisFranceNot yet recruiting
Clinique NCT + /Saint-Gatien
Coordinator of this site? Confirm its status
Saint-Cyr-sur-LoireFranceNot yet recruiting
Centre Cardiologique du Nord
Coordinator of this site? Confirm its status
Saint-DenisFranceNot yet recruiting
CHRU de Strasbourg
Coordinator of this site? Confirm its status
StrasbourgFranceNot yet recruiting
CHU de Toulouse
Coordinator of this site? Confirm its status
ToulouseFranceNot yet recruiting

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