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NCT05362656: AMPERE

AutoMatic disPERsion Tagging Function Preliminary Evaluation

Completed NA Last updated 22 November 2023
What this trial tests

NA trial testing VX1+ dispersion mapping in Atrial Fibrillation in 40 participants. Completed in 9 December 2022.

Timeline
29 May 2022
Primary endpoint
9 December 2022
9 December 2022

Quick facts

Lead sponsorVolta Medical
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment40
Start date29 May 2022
Primary completion9 December 2022
Estimated completion9 December 2022
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Volta Medical

Who can join

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

Sponsor's own description

Interventional, prospective, non-randomized, single-center, non-controlled clinical investigation as part of the premarket clinical evaluation of VX1+ medical device, aiming to verify that VX1+ in bidirectional configuration with auto-tagging function is both ergonomic and reliable for dispersed electrograms detection and automatic tagging on 3D-map in real-time.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Digital health technologies and artificial intelligence in cardiovascular clinical trials: A landscape of the European space.
    Lampreia F, Madeira C, Dores H. · · 2024 · cited 4× · PMID 39291150 · DOI 10.1177/20552076241277703

Verify or expand the search:

Other recruiting trials for Atrial Fibrillation

Currently open trials in the same condition.

Other Volta Medical 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/NCT05362656.

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