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Compares treatment options for Vasoplegia Syndrome
Official title Femoral Versus Radial Invasive Arterial Pressure Monitoring in Cardiac Surgery Patients
ClinicalTrials.gov ID: NCT06952907
What this study is testing
- What it's testing
- Background: Acute circulatory failure, often presenting as arterial hypotension, is a major contributor to postoperative morbidity and mortality. Accurate blood pressure (BP) monitoring is essential for timely therapeutic intervention, particularly in patients undergoing major surgery.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Male and female patients ≥18 years
- Scheduled cardiac surgery with cardiopulmonary bypass (time between anesthesia consultation and surgery \> 48 hours)
- ASA physical status ≥II
- Affiliation with or beneficiary of the French national health insurance system
- Signed informed consent indicating that the participant has understood the purpose and procedures of the study and agrees to participate and comply...
You likely can't join if
- Emergency surgery (before the next working day after decision to operate)
- Surgery requiring the use of two arterial pressure monitoring sites: e.g., aortic arch surgery, aortic dissection, etc.
- Heart transplantation surgery
- Mechanical circulatory support
- Contraindication to radial artery catheterization: failed Allen test, Raynaud syndrome, Buerger disease, major hyperlipidemia
- Contraindication to femoral artery catheterization: puncture of vascular prosthetic material in the femoral area (e.g., femoral bypass, femoral...
See the full eligibility criteria
- Male and female patients ≥18 years
- Scheduled cardiac surgery with cardiopulmonary bypass (time between anesthesia consultation and surgery \> 48 hours)
- ASA physical status ≥II
- Affiliation with or beneficiary of the French national health insurance system
- Signed informed consent indicating that the participant has understood the purpose and procedures of the study and agrees to participate and comply with its requirements and restrictions
- Emergency surgery (before the next working day after decision to operate)
- Surgery requiring the use of two arterial pressure monitoring sites: e.g., aortic arch surgery, aortic dissection, etc.
- Heart transplantation surgery
- Mechanical circulatory support
- Contraindication to radial artery catheterization: failed Allen test, Raynaud syndrome, Buerger disease, major hyperlipidemia
- Contraindication to femoral artery catheterization: puncture of vascular prosthetic material in the femoral area (e.g., femoral bypass, femoral stenting, femoral trifurcation endarterectomy, femoral angioplasty)
- Pregnant or breastfeeding women
- Persons deprived of liberty by judicial or administrative decision; persons under compulsory psychiatric care; persons admitted to a healthcare or social institution for reasons other than research
- Adults under legal protection measures (guardianship, trusteeship, or legal safeguard) or unable to give informed consent
- people currently under exclusion period of another clinical trial or listed in the national registry of research volunteers
The study team makes the final eligibility decision.
Where it's taking place
- Besançon, France
- Dijon, France
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Besançon, France; Dijon, France. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.