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Completed No phase listed Observational Results available

ProMRI Study of the Entovis Pacemaker System (Phase B)

ClinicalTrials.gov ID: NCT02009696

Public ClinicalTrials.gov record NCT02009696. 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 6, 2026, 8:22 AM EDT

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
NCT02009696
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Biotronik, Inc.
Industry
Enrollment
221 participants

Conditions and interventions

Interventions

  • Magnetic Resonance Imaging (MRI) scan Other
  • Patients with a ProMRI Pacemaker System Device

Other · 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
Nov 30, 2013
Primary completion
Oct 31, 2014
Completion
Dec 31, 2014
Last update posted
Nov 24, 2015

2013 – 2015

United States locations

U.S. sites
32
U.S. states
21
U.S. cities
31
Facility City State ZIP Site status
Not listed Phoenix Arizona 85018
Not listed Scottsdale Arizona 85251
Not listed Concord California 94520
Not listed Newport Beach California 92663
Not listed Rancho Mirage California 92270
Not listed New Haven Connecticut 06510
Not listed Newark Delaware 19702-5438
Not listed Washington D.C. District of Columbia 20010
Not listed Valparaiso Indiana 46383
Not listed Iowa City Iowa 52242
Not listed Lafayette Louisiana 70503
Not listed Cumberland Maryland 21502
Not listed Boston Massachusetts 02114
Not listed Burlington Massachusetts 01805
Not listed Worcester Massachusetts 01655
Not listed Ann Arbor Michigan 48109
Not listed Ypsilanti Michigan 48197
Not listed Kansas City Missouri 64132
Not listed St Louis Missouri 63110
Not listed Flushing New York 11355
Not listed New York New York 10016
Not listed The Bronx New York 10463
Not listed Winston-Salem North Carolina 27157
Not listed Toledo Ohio 43615
Not listed Salem Oregon 97301
Not listed Newtown Pennsylvania 18940
Not listed Greenville South Carolina 29605
Not listed Greenville South Carolina 29607
Not listed Amarillo Texas 79106
Not listed Mechanicsville Virginia 23116
Not listed Virginia Beach Virginia 23454
Not listed Spokane Washington 99204

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 NCT02009696, 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 Nov 24, 2015 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02009696 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →