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NCT04964440

Redo AF Sub Study (of the Pure EP 2.0 Main Study)

Completed Last updated 11 February 2022
What this trial tests

trial testing Pure-EP in Atrial Fibrillation Recurrent in 20 participants. Completed in 29 January 2022.

Timeline
3 March 2021
Primary endpoint
20 July 2021
29 January 2022

Quick facts

Lead sponsorBioSig Technologies, Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment20
Start date3 March 2021
Primary completion20 July 2021
Estimated completion29 January 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

BioSig Technologies, Inc.

Who can join

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

Sponsor's own description

This study is a sub study of the Pure EP 2.0 trial. In a redo atrial fibrillation population, this study is designed to collect pulmonary vein signals pre and post ablation therapy, along with other non-pulmonary vein signals of interest during a redo ablation procedure. These signals are later evaluated for clinical relevance and impact on the procedure.

Publications & conference data

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

Verify or expand the search:

Other recruiting trials for Atrial Fibrillation Recurrent

Currently open trials in the same condition.

Other BioSig Technologies, Inc. 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/NCT04964440.

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