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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 Oct 20, 2026, 8:58 PM EDT

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of the ProMRI Study (Phase B) is to demonstrate the clinical safety of the ProMRI Pacemaker System when used under specific MRI conditions without scan exclusion zone.

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

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
Dec 2013 (Type not available)
Primary completion
Nov 2014 (Actual)
Completion
Jan 2015 (Actual)
Last update posted
Nov 25, 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 25, 2015 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02009696 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →