Actively Recruiting
Assessing Fluid-responsiveness Using Non-invasive Hybrid Diffuse Optics on Peripheral Muscle
Led by Corporacion Parc Tauli · Updated on 2026-03-18
200
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
C
Corporacion Parc Tauli
Lead Sponsor
I
Institut de Ciències Fotòniques (ICFO)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This observational study focuses on critically ill patients in intensive care who have invasive blood pressure monitoring through an arterial line. It aims to evaluate the relationship between cardiac output and microvascular blood flow in peripheral muscles during a Passive Leg Raising (PLR) maneuver. Researchers will assess how microvascular measurements correlate with cardiac output changes and their ability to predict positive cardiac output responses. Participants will undergo a PLR maneuver where their lower limbs are elevated to a 45° angle while the upper body moves from a semi-recumbent to supine position for three minutes before returning to the initial position. During this procedure, microvascular blood flow and tissue oxygen saturation will be measured on the brachioradialis muscle using the hybrid diffuse optics spectroscopy (hDOS) platform. Cardiac output will be monitored invasively through the arterial line using pulse waveform analysis. Throughout the study, researchers will collect data on cardiac output response during the PLR procedure and monitor microvascular parameters over time. This includes measuring blood flow index and tissue oxygen saturation. The study will assess these variables' potential to predict cardiac output increases greater than 10%. The total duration of participant involvement and follow-up details are not specified.
CONDITIONS
Brief Title
Assessing Fluid-responsiveness Using Non-invasive Hybrid Diffuse Optics on Peripheral Muscle
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Invasive blood pressure monitoring through an arterial line
You will not qualify if you...
- Patients with suspected pregnancy
- Intra-abdominal hypertension
- Elevated intracranial pressure
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single assessment during the procedure
Participants undergo the Passive Leg Raising maneuver while being monitored for cardiac output response.
1 visit (in-person)
Duration - Duration varies based on clinical monitoring
Participants are observed following the procedure to assess outcomes over time.
Visit frequency depends on clinical care
Trial Site Locations
Total: 1 location
1
Parc Taulí Hospital Universitari
Sabadell, Spain/ Barcelona, Spain, 08208
Actively Recruiting
Research Team
J
Jaume Mesquida Senior Clinical Researcher, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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