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NCT03987204

Ivabradine for Rate Control in Permanent Atrial Fibrillation

Completed Phase 1 Last updated 2 July 2021
What this trial tests

Phase 1 trial testing Ivabradine in Atrial Fibrillation in 4 participants. Completed in 17 September 2019.

Timeline
15 June 2019
Primary endpoint
17 September 2019
17 September 2019

Quick facts

Lead sponsorYale University
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment4
Start date15 June 2019
Primary completion17 September 2019
Estimated completion17 September 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Yale University

Who can join

Adults 21 to 90, any sex, with Atrial Fibrillation or Atrial Fibrillation, Persistent. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Ivabradine may be useful as a rate controlling agent in atrial fibrillation without negative effects on hemodynamics and inotropy. The objective in this proof of concept study is to investigate the hypothesis that ivabradine will slow the ventricular response in patients with permanent atrial fibrillation and previously-implanted pacemakers.

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 trials of Ivabradine

Trials testing the same drug.

Other recruiting trials for Atrial Fibrillation

Currently open trials in the same condition.

Other Yale University 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/NCT03987204.

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