Heart rate and respiration monitoring device: performance and usability in patients of all ages

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study collects ECG and respiration data from participants across age groups to evaluate a new monitoring technology. The goal is to assess performance, usability, and safety in real-world clinical settings. Data will support device development, documentation of safety and performance, and regulatory compliance. No intervention is applied beyond data collection during routine hospital care.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Able to provide written informed consent or have a Legally Designated Representative (LDR) to provide written informed consent;
2. Are being cared for in a hospital unit and are expected to remain in the unit for the duration of the study procedure; AND
3. ECG can be collected

Exclusion Criteria:

1. Are known to be pregnant\*
2. Are breastfeeding; OR,
3. Are suffering from infection(s) or immunocompromised patients that require isolation.
4. PI or caring physician decision due to subject health condition

Where it's running

• Helsinki University Hospital
  Espoo, Finland Recruiting

Study contacts

• Study coordinator: Tero Varpula Principal Investigator
• Email: tero.varpula@hus.fi
• Phone: +35894711

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.