NCT06783868Not yet recruiting
Assessing the Neurological Outcomes After Atrial Fibrillation Ablation for Rhythm Control
Randomized Control Study to Assess the Neurological Outcomes After Atrial Fibrillation Ablation for Rhythm Control vs Routine Medication Therapy in Patients With Recent Stroke: SAVE STROKE Phase II Study
Source: ClinicalTrials.gov · Last updated 28 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
A prospective, non-blinded, multi-center study to assess the impact of early Catheter Ablation (CA) in patients with a new diagnosis of Atrial Fibrillation(AF) at the time of stroke. 100 patients will be enrolled.
- Status (registry)
- Not yet recruiting
- Study type
- Observational
- Enrollment
- 100 (estimated)
- First submitted
- 14 Jan 2025
- Start date
- Oct 2025
- Primary completion date
- Jun 2027
- Lead sponsor
- Kansas City Heart Rhythm Research Foundation
- Diseases
- Stroke, Atrial fibrillation
- NCT number
- NCT06783868
What you commit to
- Study type: Observational
- Planned participants: 100
- From Oct 2025 to the primary completion date, Jun 2027
- 7 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Age
- Patients \< 18 years of age
Other
- Unable to provide consent, including mRS = 6.
- Not able to read and write at an 8th-grade level \[to complete AFEQT and EQ-5D surveys\]
- Positive B-hCG
- Will not follow up with our practice/clinic afterward.
- Cannot tolerate OAC or AAD for any reason.
- Cannot undergo CA for any reason.
Who the study is looking for
- Ages \>18 and able to provide consent.
- Presenting with an acute stroke and new-onset AF
- Modified RANKIN score (mRS) \< 6
- Must be able to undergo some form of cardiac monitoring \[implantable loop recorder (ILR), electrocardiogram (ECG), Holter monitor\] to quantify AF burden
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (7)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Centerpoint Medical Center Clinic Coordinator of this site? Confirm its status | Independence | United States | Unknown status |
| Centerpoint Medical Center Coordinator of this site? Confirm its status | Independence | United States | Unknown status |
| Research Medical Center Coordinator of this site? Confirm its status | Kansas City | United States | Unknown status |
| Research Medical Center Clinic Coordinator of this site? Confirm its status | Kansas City | United States | Unknown status |
| Overland Park Regional Medical Center Coordinator of this site? Confirm its status | Overland Park | United States | Unknown status |
| Menorah Medical Center Coordinator of this site? Confirm its status | Overland Park | United States | Unknown status |
| Kansas City Heart Rhythm Institute - Roe Clinic Coordinator of this site? Confirm its status | Overland Park | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.