Apixaban Evaluation of Interrupted Or Uninterrupted Anticoagulation for Ablation of Atrial Fibrillation
Public ClinicalTrials.gov record NCT02608099. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Study identification
- NCT ID
- NCT02608099
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 4
- Lead sponsor
- Baim Institute for Clinical Research
- Other
- Enrollment
- 300 participants
Conditions and interventions
Conditions
Interventions
- Interrupted apixaban Drug
- Uninterrupted apixaban Drug
Drug
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Oct 31, 2015
- Primary completion
- Mar 31, 2017
- Completion
- Mar 31, 2017
- Last update posted
- Mar 16, 2020
2015 – 2017
United States locations
- U.S. sites
- 19
- U.S. states
- 16
- U.S. cities
- 19
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Site 0020 | Huntsville | Alabama | 35801 | — |
| Site 0005 | Mission Viejo | California | 92690 | — |
| Site 0012 | New Haven | Connecticut | 06501 | — |
| Site 0011 | Trumbull | Connecticut | 06611 | — |
| Site 0016 | Pensacola | Florida | 32501 | — |
| Site 0014 | West Des Moines | Iowa | 50266 | — |
| Site 0018 | Bangor | Maine | 04401 | — |
| Site 0004 | Scarborough | Maine | 04074 | — |
| Site 0008 | Boston | Massachusetts | 02118 | — |
| Site 0001 | Burlington | Massachusetts | 01805 | — |
| Site 0006 | Kansas City | Missouri | 64111 | — |
| Site 0021 | Omaha | Nebraska | 68131 | — |
| Site 0019 | Albuquerque | New Mexico | 87101 | — |
| Site 0002 | Toledo | Ohio | 43615 | — |
| Site 0007 | Oklahoma City | Oklahoma | 73104 | — |
| Site 0009 | Philadelphia | Pennsylvania | 19019 | — |
| Site 0010 | Charleston | South Carolina | 29401 | — |
| Site 0017 | Austin | Texas | 78705 | — |
| Site 0003 | Richmond | Virginia | 23219 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT02608099, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Mar 16, 2020 · Synced Jul 21, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT02608099 live on ClinicalTrials.gov.