Dynamic Data-Driven Management of Atrial Fibrillation Using Implantable Cardiac Monitors: The MONITOR-AF Study
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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT06352060. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.
All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
Observational, multi-center, retrospective study to evaluate the use of ICM (implantable cardiac monitor) versus traditional, non-ICM (non-implantable cardiac monitor) methods such as ECGs (electrocardiogram), Holter, and mobile cardiac outpatient telemetry (MCOT) units.
Study identification
- NCT ID
- NCT06352060
- Recruitment status
- Completed
- Study type
- Observational
- Phase
- Not listed
- Enrollment
- 598 participants
Conditions and interventions
Conditions
Interventions
- No intervention or administration will be performed due to the observational nature of the study Other
Other
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
- Jan 1, 2018 (Actual)
- Primary completion
- Dec 31, 2021 (Actual)
- Completion
- Dec 31, 2021 (Actual)
- Last update posted
- Apr 18, 2025
2018 – 2021
United States locations
- U.S. sites
- 7
- U.S. states
- 2
- U.S. cities
- 3
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Menorah Medical Center | Overland Park | Kansas | 66209 | — |
| Kansas City Heart Rhythm Institute - Roe Clinic | Overland Park | Kansas | 66211 | — |
| Overland Park Regional Medical Center | Overland Park | Kansas | 66215 | — |
| Centerpoint Medical Center Clinic | Independence | Missouri | 64057 | — |
| Centerpoint Medical Center | Independence | Missouri | 64057 | — |
| Research Medical Center Clinic | Kansas City | Missouri | 64032 | — |
| Research Medical Center | Kansas City | Missouri | 64032 | — |
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 NCT06352060, 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 Apr 18, 2025 · Synced Nov 14, 2026
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