Trial · NCT00215774
Flecainide-Short Long Study (Flec-SL)
NCT00215774, Not applicable, Completed, Atrial Fibrillation Network
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Flecainide-Short Long Study (Flec-SL). Trials, record NCT00215774. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00215774
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Flecainide-Short Long Study (Flec-SL)
- NCT number
- NCT00215774
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 760 participants, actual
- Lead sponsor
- Atrial Fibrillation Network
- Conditions
- Atrial Fibrillation
- Interventions
- Flecainide
- First posted
- 2005-09-22
- Last updated
- 2012-09-11
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | time to persistent atrial fibrillation as determined by daily telemetric ECG recordings and verified by Holter ECG recording | primary endpoint | |
| Secondary | time to first symptomatic episode of AF | end of trial | |
| Secondary | AF burden (number and duration of AF episodes) | end of trial | |
| Secondary | number of hospitalizations due to AF | end of trial | |
| Secondary | time to termination of trial medication | end of trial | |
| Secondary | number of serious adverse events including pro-arrhythmic events | end of trial | |
| Secondary | quality of life | end of trial |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers3
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT00215774
GET https://conductscience.org/api/trials/v1/NCT00215774/registered