Measurement of the sublingual microcirculation in critically ill children at the bedside: a pilot study

Measurement of the sublingual microcirculation in critically ill children at the bedside: a pilot study - sequential measurement microcirculation

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON55784

Enrollment

Registered

2019-10-04

Start date

2019-12-12

Completion date

Unknown

Last updated

2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

microcirculatie microcirculation

Interventions

None listed

Eligibility

Age

2 Years to 17 Years

Inclusion criteria

Inclusion criteria: -mechanically ventilation for at least 24 hours -sedation -0-18 years

Exclusion criteria

Exclusion criteria: -no written informed consent from both parents

Design outcomes

Secondary

Measure	Time frame
The second aim is to design a more practical way to analyze and interpret the microcirculatory bedside derived datasets. Sublingual microcirculatory measurements will be evaluated with a CytoCam, an optical spectroscopic sensor-based digital video imaging instrument (Braedius Medical BV, The Netherlands). Sublingual microcirculation profile consists of blood vessel diameter (BVd), proportion of perfused vessels (PVV), perfused vessel density (PVD), microcirculatory flow index (MFI) and total vascular density (TVD).	—

Measure

Time frame

The second aim is to design a more practical way to analyze and interpret the microcirculatory bedside derived datasets. Sublingual microcirculatory measurements will be evaluated with a CytoCam, an optical spectroscopic sensor-based digital video imaging instrument (Braedius Medical BV, The Netherlands). Sublingual microcirculation profile consists of blood vessel diameter (BVd), proportion of perfused vessels (PVV), perfused vessel density (PVD), microcirculatory flow index (MFI) and total vascular density (TVD).

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Primary

Measure	Time frame
The primary study parameter is to determine the within-patient reproducibility of the sequential measurement of the microcirculatory region of interest in critically ill children.	—

Countries

Netherlands

Outcome results