The use of an external ultrasound fixator (ProbeFix) on Intensive Care patients, a feasibility study.

The use of an external ultrasound fixator (ProbeFix) on Intensive Care patients, a feasibility study. - SOUNDPROBE

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON44443

Enrollment

Registered

2018-01-08

Start date

2018-05-17

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

change in cardiac ouput

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Adult Intensive Care patients ( > 18 years), with hypovolemia detected with Flotrac (SVV > 10%)

Exclusion criteria

Exclusion criteria: Pregnancy Atrial fibrillation or other irregular heart rhythm Pulmonary edema PLR not possible (eg neurological disease, spinal trauma, restricted limb movement, deep venous thrombosis, or any other reason as indicated by the attending intensivist). age

Design outcomes

Primary

Measure	Time frame
1. Correlation between cardiac output measurements with and without ProbeFix with Flotrac measurements 2. percentage of patients in which the ProbeFix can be used	—

Secondary

Measure	Time frame
1. Signs of side effects of ProbeFix 2. If possible patients will be asked to rate the (un)comfort of the ProbeFix	—

Countries

Netherlands

Outcome results