Examining the Aortic to Radial Pressure Gradient in Shock Conditions

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study investigates the prevalence of the aortic to radial pressure gradient (ATRAP) in patients experiencing shock outside of cardiac surgery. It aims to measure the pressure differences between the radial and femoral arteries to understand the implications for vasopressor administration. The study includes patients who are on vasopressor support and have invasive blood pressure monitoring in place. By identifying the ATRAP, the research seeks to improve patient management in intensive care settings.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* age superior or equal 18 years
* Vasopressors support superior or equal 0.5 µg/kg/min of equivalent norepinephrine
* Invasive monitoring of blood pressure with a radial arterial catheter and a femoral arterial catheter decided by de physician
* Beginning of the shock less than 48 hours.
* Consent

Exclusion Criteria:

* perioperative of cardiac surgery (between the beginning of the surgery and 7 days after)
* pregnant woman or breast-feeding
* Major person under protection
* Person with privation of liberty by a justice decision, or an administrative decision

Where it's running

• Département d'anesthésie Réanimation Hôpital Cardiologique Louis Pradel/Groupement Hospitalier Est
  Bron, France Recruiting
• Département d'anesthésie-réanimation CHU de Clermont-Ferrand
  Clermont-Ferrand, France Recruiting
• Service d'Anesthésie Association hospitalière Protestante de Lyon
  Lyon, France Recruiting
• Hopital Edouard heriot/Groupement hospitalier Centre, service de médecine intensive réanimation
  Lyon, France Recruiting
• Hôpital Edouard Heriot/ Groupement hospitalier Centre, service d'anesthésie réanimation
  Lyon, France Recruiting
• Hôpital de la Croix-Rousse/Groupement hospitalier Nord, service d'anesthésie réanimation
  Lyon, France Recruiting

Study contacts

• Study coordinator: Matthias Jacquet-lagreze, Dr
• Email: matthias.jacquet-lagreze@chu-lyon.fr
• Phone: 0783426888

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.