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New treatment option for Hemodynamics
Official title Non-Invasive Blood Pressure Monitoring in ICU Patients Using the DARE Device
ClinicalTrials.gov ID: NCT07052123
What this study is testing
- What it's testing
- This study tests a new non-invasive device called DARE to monitor blood pressure in patients in intensive care. It compares the device's readings to standard invasive methods and also looks at how well it measures other vital signs like temperature, oxygen levels, and heart rhythm.
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
- Adult patients (male or female), aged 18 years or older
- Admitted to intensive care unit (ICU) or critical care with an expected hospital stay longer than 2 days
- Equipped with an arterial catheter for invasive blood pressure monitoring
- Equipped with a urinary catheter for invasive core body temperature monitoring
You likely can't join if
- Patients under 18 years old (minors)
- Known skin allergy to adhesives or silicone, or skin condition preventing adhesive use
- History of extensive skin pathology (e.g., Lyell syndrome)
- Patients with therapeutic limitations
- Patients with active implanted medical devices (e.g., pacemaker, defibrillator)
- Pregnant or breastfeeding women
See the full eligibility criteria
- Adult patients (male or female), aged 18 years or older
- Admitted to intensive care unit (ICU) or critical care with an expected hospital stay longer than 2 days
- Equipped with an arterial catheter for invasive blood pressure monitoring
- Equipped with a urinary catheter for invasive core body temperature monitoring
- Patients under 18 years old (minors)
- Known skin allergy to adhesives or silicone, or skin condition preventing adhesive use
- History of extensive skin pathology (e.g., Lyell syndrome)
- Patients with therapeutic limitations
- Patients with active implanted medical devices (e.g., pacemaker, defibrillator)
- Pregnant or breastfeeding women
- Patients not affiliated with the French social security system
- Patients or their legal representatives refusing consent, or unable to understand information and give informed consent
- Patients under legal guardianship, curatorship, or deprived of liberty
The study team makes the final eligibility decision.
Where it's taking place
- Saint-Denis, France, 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 Saint-Denis, France, 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.