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NCT03964025

Clinical Investigation to Determine the Accuracy and Benefit of Cardioskin™ in Patients With Known Atrial Fibrillation

Withdrawn NA Last updated 7 May 2021
What this trial tests

NA trial testing Wearing Cardioskin™ for 14 days in Atrial Fibrillation. Withdrawn.

Timeline
1 July 2021
Primary endpoint
1 January 2022
1 January 2022

Quick facts

Lead sponsorInstitut de Recherches Internationales Servier
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposesupportive care
Start date1 July 2021
Primary completion1 January 2022
Estimated completion1 January 2022
Sites3 locations across Netherlands

Drugs / interventions tested

Conditions studied

Sponsor

Institut de Recherches Internationales Servier — full company profile →

Who can join

18 and older, any sex, with Atrial Fibrillation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a prospective, non-randomized, comparative, single-arm, open label, multi- centre, post-market clinical investigation involving an expected 74 subjects (minimum 40, maximum 118) suffering from paroxysmal AF with the aim to determine the accuracy of "definitive" AF detection (≥30 seconds) of the Cardioskin™ as compared to a 3-lead Holter recorder in patients with known paroxysmal AF.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Atrial Fibrillation

Currently open trials in the same condition.

Other Institut de Recherches Internationales Servier trials

Trials by the same sponsor.

Verify against primary sources

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/NCT03964025.

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