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NCT06683183

Ability of the Polar Wearables to Detect Fetal Heart Rate - Pilot Clinical Study

Completed Last updated 18 April 2025
What this trial tests

trial in Fetal Heart Rate Tracing in 11 participants. Completed in 11 April 2025.

Timeline
19 February 2025
Primary endpoint
11 April 2025
11 April 2025

Quick facts

Lead sponsorAnna Axelin
StatusCompleted
Study typeOBSERVATIONAL
Enrollment11
Start date19 February 2025
Primary completion11 April 2025
Estimated completion11 April 2025
Sites1 location across Finland

Conditions studied

Sponsor

Anna Axelin

Who can join

Eligibility, female only, with Fetal Heart Rate Tracing. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this clinical pilot study is 1. to evaluate the ability of the wearables to detect fetal heart rate 2. to evaluate the ability to distinguish the fetal ECG from the ECG of the mother The participating pregnant women will wear the Polar wearables (chest band, smart watch, arm band) for 15 minutes during of which, the data will be collected with all three wearables and patient monitor (reference device). The data from the wearables will be compared with the patient monitor data referred as golden standard. Background information will be collected with questionnaires from the participants. The data collection will be conducted in hospital environment.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Anna Axelin trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06683183.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing