Actively Recruiting

Age: 18Years +
All Genders
ID07298720

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Invasive blood pressure monitoring through an arterial line
Not Eligible

You will not qualify if you...

  • Patients with suspected pregnancy
  • Intra-abdominal hypertension
  • Elevated intracranial pressure

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Single assessment during the procedure

Participants undergo the Passive Leg Raising maneuver while being monitored for cardiac output response.

1 visit (in-person)

Long-term Monitoring

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

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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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