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Completed Not applicable Interventional Results available

PREFER (Pacemaker Remote Follow-Up Evaluation and Review)

ClinicalTrials.gov ID: NCT00294645

Public ClinicalTrials.gov record NCT00294645. 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 Jul 22, 2026, 3:47 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

Pacemaker Remote Follow-up Evaluation and Review

Study identification

NCT ID
NCT00294645
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Medtronic Cardiac Rhythm and Heart Failure
Industry
Enrollment
980 participants

Conditions and interventions

Interventions

  • Transtelephonic monitoring (TTM) Other
  • Medtronic CareLink® Network Other

Other

Eligibility (public fields only)

Age range
Not listed
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
Mar 31, 2004
Primary completion
Mar 31, 2008
Completion
Mar 31, 2008
Last update posted
Oct 18, 2010

2004 – 2008

United States locations

U.S. sites
45
U.S. states
29
U.S. cities
45
Facility City State ZIP Site status
Not listed Scottsdale Arizona
Not listed Little Rock Arkansas
Not listed Washington D.C. District of Columbia
Not listed Ormond Beach Florida
Not listed Safety Harbor Florida
Not listed Springfield Illinois
Not listed Des Moines Iowa
Not listed Lafayette Louisiana
Not listed Bangor Maine
Not listed Glen Burnie Maryland
Not listed Takoma Park Maryland
Not listed Burlington Massachusetts
Not listed Ann Arbor Michigan
Not listed Minneapolis Minnesota
Not listed Hattiesburg Mississippi
Not listed Jackson Mississippi
Not listed Kansas City Missouri
Not listed St Louis Missouri
Not listed Great Falls Montana
Not listed Omaha Nebraska
Not listed Reno Nevada
Not listed Ocean City New Jersey
Not listed Paterson New Jersey
Not listed Towaco New Jersey
Not listed Voorhees Township New Jersey
Not listed Mineola New York
Not listed Raleigh North Carolina
Not listed Cleveland Ohio
Not listed Columbus Ohio
Not listed Dayton Ohio
Not listed Marion Ohio
Not listed Tulsa Oklahoma
Not listed Bend Oregon
Not listed Lancaster Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Wynnewood Pennsylvania
Not listed Columbia South Carolina
Not listed Chattanooga Tennessee
Not listed Nashville Tennessee
Not listed Corpus Christi Texas
Not listed Houston Texas
Not listed Plano Texas
Not listed Temple Texas
Not listed Tacoma Washington
Not listed Wauwatosa Wisconsin

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 NCT00294645, 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 Oct 18, 2010 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00294645 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →