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NCT00408473
Comparative Study of Flecainide CR and Placebo in the Early Treatment of Atrial Fibrillation.
Phase 4 trial testing Flecainide in Atrial Fibrillation in 256 participants. Terminated before completion.
Quick facts
| Lead sponsor | MEDA Pharma GmbH & Co. KG |
|---|---|
| Phase | Phase 4 |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 256 |
| Sites | 47 locations across France, Netherlands, Belgium, Germany, Romania, Bulgaria, Spain |
Drugs / interventions tested
- Flecainide (FLECAINIDE) — full drug profile →
Conditions studied
- Atrial Fibrillation — all drugs for Atrial Fibrillation →
Sponsor
MEDA Pharma GmbH & Co. KG — full company profile →
Who can join
Adults 18 to 65, any sex, with Atrial Fibrillation. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of the study is to assess the efficacy of flecainide controlled release (CR) in the prevention of recurrent AF during 9 months of active treatment compared to placebo in patients with only one documented AF episode.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Tic-Tac: A Translational Approach in Mechanisms Associated with Irregular Heartbeat and Sinus Rhythm Restoration in Atrial Fibrillation Patients.
Parra-Lucares A, Villa E, Romero-Hernández E, Méndez-Valdés G, et al · · 2023 · PMID 37629037 · DOI 10.3390/ijms241612859
Verify or expand the search:
- PubMed search for NCT00408473
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Flecainide
Trials testing the same drug.
- NCT06142604 — Single Dose Flecainide for Early Sinus Rhythm Conversion of Perioperative Atrial Fibrillation After Noncardiac Surgery · Phase 4 · withdrawn
- NCT04837261 — Shortening Duration of Antiarrhythmic Medication for SVT in Infants · completed
- NCT02347111 — Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation · Phase 4 · recruiting
- NCT03587558 — Effects of Carvedilol on Suppressing the Premature Ventricular Complex/Ventricular Tachycardia From Outflow Tract · Phase 4 · unknown
Other recruiting trials for Atrial Fibrillation
Currently open trials in the same condition.
- NCT07429214 — A Study of VARIPULSE Catheter and TRUPULSE Generator With VARIPULSE Pro Software in Participants With PAF or PsAF · NA · recruiting
- NCT07271238 — Feasibility Study on the VERAFEYE Imaging and Navigation System for Guided Catheter Ablation Procedures · NA · recruiting
- NCT07388108 — Atrial Dyssynchrony to Predict Arrhythmias in the Postoperative Setting of Cardiovascular Surgery. · recruiting
- NCT07428967 — AV Node Ablation and CONDUCTion System Pacing for Atrial Fibrillation With Preserved Left Ventricular Function · NA · recruiting
- NCT06650995 — AlEX-DHF: Ablation and Exercise in Diastolic Heart Failure · NA · recruiting
Other MEDA Pharma GmbH & Co. KG trials
Trials by the same sponsor.
- NCT06126952 — Azelastine Allergen Chamber - Onset of Action Study · Phase 2 · completed
- NCT05544695 — Real-world Evidence Study on Cystistat · completed
- NCT04652245 — Dymista Allergen Chamber - Onset of Action Study · Phase 4 · completed
- NCT03599791 — DYmista NAsal Spray in CHInese Patients · Phase 3 · completed
- NCT03004131 — MP-AzeFlu Allergen Chamber - Onset of Action Study · Phase 4 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00408473 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by MEDA Pharma GmbH & Co. KG
- Last refreshed: 7 February 2022
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/NCT00408473.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing