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Completed Not applicable Interventional

Clinical Investigation of the SelectSecure Pacing Lead

ClinicalTrials.gov ID: NCT00266682

Public ClinicalTrials.gov record NCT00266682. 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 7, 2026, 7:59 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.

People who have a slow heart beat, or whose heart does not beat on its own, may be in need of an electronic device called a pacemaker. A pacemaker is implanted surgically just under the skin in the upper chest area. This device helps the heart beat at a regular rhythm by sending electrical signals (pacing) directly to the heart tissue through flexible wires called leads. The purpose of this study is to demonstrate that the SelectSecure (Model 3830) lead is safe and effective for both sensing the heart's natural rhythm and pacing the heart when it does not beat on its own. This lead will be studied in both the right atrium and right ventricle. A previously market approved Medtronic lead model will serve as a comparison to prove the safety and effectiveness of the SelectSecure Model.

Study identification

NCT ID
NCT00266682
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
365 participants

Conditions and interventions

Conditions

Interventions

Device

Eligibility (public fields only)

Age range
0 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
Jul 31, 2002
Primary completion
Not listed
Completion
Jul 31, 2005
Last update posted
Oct 12, 2006

2002 – 2005

United States locations

U.S. sites
26
U.S. states
19
U.S. cities
26
Facility City State ZIP Site status
Not listed Anchorage Alaska
Not listed Peoria Arizona
Not listed Long Beach California
Not listed Santa Rosa California
Not listed Fort Lauderdale Florida
Not listed Evanston Illinois
Not listed Indianapolis Indiana
Not listed Des Moines Iowa
Not listed Iowa City Iowa
Not listed Kansas City Kansas
Not listed Boston Massachusetts
Not listed Detroit Michigan
Not listed Robbinsdale Minnesota
Not listed Saint Paul Minnesota
Not listed Kansas City Missouri
Not listed Springfield Missouri
Not listed Livingston New Jersey
Not listed Winston-Salem North Carolina
Not listed Cincinnati Ohio
Not listed Lancaster Pennsylvania
Not listed Sayre Pennsylvania
Not listed Germantown Tennessee
Not listed Nashville Tennessee
Not listed Austin Texas
Not listed Temple Texas
Not listed Richmond Virginia

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00266682, 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 12, 2006 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00266682 live on ClinicalTrials.gov.

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