Assessing Fluid-responsiveness Using Non-invasive Hybrid Diffuse Optics on Peripheral Muscle

Recruiting Observational Study
Critical Illness
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
200 (estimated)
Sponsor
Corporacion Parc Tauli · Other
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About This Trial
Proof-of-concept observational study including ICU patients undergoing a PLR maneuver. Local microvasculature will be assessed with the hDOS platform on the brachioradialis muscle, deriving the microvascular blood flow index (BFI) and tissue oxygen saturation (StO2). CO will be assessed via an invasive hemodynamic monitor based on pulse waveform analysis through the patient's arterial line. The co…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Invasive blood pressure monitoring through an arterial line Exclusion Criteria: * Patients with suspected pregnancy * Intra-abdominal hypertension * Elevated intracranial pressure
Contacts

Jaume Mesquida Senior Clinical Researcher, MD

+34 616722287

jmesquida@tauli.cat

CONTACT