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Completed No phase listed Observational Results available

ProMRI Study of the Entovis Pacemaker System

ClinicalTrials.gov ID: NCT01761162

Public ClinicalTrials.gov record NCT01761162. 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 26, 2026, 12:00 AM 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 is to demonstrate the clinical safety of the ProMRI Pacemaker System when used under specific MRI conditions.

Study identification

NCT ID
NCT01761162
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Biotronik, Inc.
Industry
Enrollment
229 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
Feb 2013 (Type not available)
Primary completion
Mar 2014 (Actual)
Completion
May 2014 (Actual)
Last update posted
Feb 9, 2017

2013 – 2014

United States locations

U.S. sites
25
U.S. states
19
U.S. cities
25
Facility City State ZIP Site status
Arizona Arrhythmia Consultants Scottsdale Arizona 85251 —
John Muir Medical Center Concord California 94520 —
Hoag Hospital Newport Beach California 92663 —
Eisenhower Medical Center Rancho Mirage California 92270 —
Yale - New Haven Hospital New Haven Connecticut 06510 —
Washington Hospital Center Washington D.C. District of Columbia 20010 —
Not listed Valparaiso Indiana 46383 —
University of Iowa Hospitals and Clinics Iowa City Iowa 52242 —
Louisiana Heart Rhythm Specialists Lafayette Louisiana 70503 —
Not listed Cumberland Maryland 21502 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Not listed Burlington Massachusetts 01805 —
University of Massachusetts Medical School Worcester Massachusetts 01655 —
Saint Joseph Mercy Medical Center Ypsilanti Michigan 48197 —
Research Medical Center Kansas City Missouri 64132 —
Washington University St Louis Missouri 63110 —
Not listed Camden New Jersey 08103 —
New York Hospital Queens Flushing New York 11355 —
Not listed New York New York 10016 —
Not listed Winston-Salem North Carolina 27157 —
Toledo Hospital Toledo Ohio 46306 —
Saint Mary Medical Center Langhorne Pennsylvania 19047 —
Rhode Island Hospital Providence Rhode Island 02903 —
Not listed Greenville South Carolina 29601 —
Not listed Richmond Virginia 23230 —

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 NCT01761162, 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 Feb 9, 2017 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01761162 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →