ClinicalTrials.gov record
Active, not recruiting No phase listed Observational

SPHERE Per-AF Post-Approval Study

ClinicalTrials.gov ID: NCT06858306

Public ClinicalTrials.gov record NCT06858306. 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.

ClinicalTrials.gov public records Last synced May 19, 2026, 6:31 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

SPHERE Per-AF Post-Approval Study, an Addendum to the Affera Global Registry

Study identification

NCT ID
NCT06858306
Recruitment status
Active, not recruiting
Study type
Observational
Phase
Not listed
Lead sponsor
Medtronic Cardiac Ablation Solutions
Industry
Enrollment
200 participants

Conditions and interventions

Interventions

  • Sphere-9™ Catheter and Affera™ Ablation System Device

Device

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
Sep 24, 2025
Primary completion
Sep 30, 2030
Completion
Sep 30, 2030
Last update posted
May 7, 2026

2025 – 2030

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
University of Alabama at Birmingham Hospital Birmingham Alabama 35294
Sarasota Memorial Hospital Sarasota Florida 34239
Piedmont Heart Institute Atlanta Georgia 30309
Minneapolis Heart Institute Foundation Minneapolis Minnesota 55407
Mayo Clinic Rochester Minnesota 55905
Montefiore Medical Center New York New York 10467
Atrium Health Carolinas Medical Center Charlotte North Carolina 28230
OhioHealth Columbus Ohio 43214
Doylestown Health Cardiology Doylestown Pennsylvania 18901
Allegheny General Hospital Pittsburgh Pennsylvania 15212
Texas Health Resources Fort Worth Texas 76104
Houston Methodist Hospital Houston Texas 77030
University of Virginia Medical Center Charlottesville Virginia 22903
Centra Medical Group Stroobants Cardiovascular Center Lynchburg Virginia 24501

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 NCT06858306, 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 May 7, 2026 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06858306 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →