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Completed No phase listed Observational Results available

ProMRI Study of the Iforia ICD System (Phase C)

ClinicalTrials.gov ID: NCT02096692

Public ClinicalTrials.gov record NCT02096692. 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 Sep 1, 2026, 11:08 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 is to demonstrate the clinical safety of the ProMRI ICD System when used under specific MRI conditions.

Study identification

NCT ID
NCT02096692
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Biotronik, Inc.
Industry
Enrollment
154 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
May 31, 2014
Primary completion
Feb 28, 2015
Completion
May 31, 2015
Last update posted
Feb 28, 2016

2014 – 2015

United States locations

U.S. sites
39
U.S. states
23
U.S. cities
38
Facility City State ZIP Site status
Not listed Birmingham Alabama 35294
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
Not listed Washington D.C. District of Columbia 20010
Not listed Valparasio Indiana 46383
Not listed Iowa City Iowa 52242
Not listed Lafayette Louisiana 70503
Not listed Cumberland Maryland 21502
Not listed Takoma Park Maryland 20912
Not listed Boston Massachusetts 02114
Not listed Burlington Massachusetts 01805
Not listed Worcester Massachusetts 01655
Not listed Ann Arbor Michigan 48109
Not listed Grand Rapids Michigan 49506
Not listed Ypsilanti Michigan 48197
Not listed Kansas City Missouri 94520
Not listed St Louis Missouri 63110
Not listed Flushing New York 11355
Not listed New York New York 10016
Not listed New York New York 10021
Not listed The Bronx New York 10463
Not listed Winston-Salem North Carolina 27157
Not listed Columbus Ohio 43210
Not listed Toledo Ohio 43615
Not listed Portland Oregon 97225
Not listed Salem Oregon 97301
Not listed Langhorne Pennsylvania 08691
Not listed Wynnewood Pennsylvania 19096
Not listed Greenville South Carolina 29615
Not listed Nashville Tennessee 37232
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 NCT02096692, 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 28, 2016 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02096692 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →