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Completed Not applicable Interventional Results available

Attain Model 4196 Left Ventricular (LV) Lead

ClinicalTrials.gov ID: NCT00271544

Public ClinicalTrials.gov record NCT00271544. 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 29, 2026, 9:47 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.

Heart failure is a progressive disease that decreases the pumping action of the heart. This may cause a backup of fluid in the heart and may result in heart beat changes. When there are changes in the heart beat sometimes an implantable heart device is used to control the rate and rhythm of the heart beat. In certain heart failure cases, when the two lower chambers of the heart no longer beat in a coordinated manner, cardiac resynchronization therapy (CRT) may be prescribed. CRT is similar to a pacemaker. It is placed (implanted) under the skin of the upper chest. CRT is delivered as tiny electrical pulses to the right and left ventricles through three or four leads (flexible insulated wires) that are inserted through the veins to the heart. The purpose of this study is to evaluate a new lead for delivering energy to the left ventricle (bottom left chamber of the heart).

Study identification

NCT ID
NCT00271544
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
190 participants

Conditions and interventions

Conditions

Interventions

Device

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 2007 (Type not available)
Primary completion
Aug 2007 (Actual)
Completion
Dec 2008 (Actual)
Last update posted
Sep 28, 2009

2007 – 2008

United States locations

U.S. sites
19
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Not listed Anchorage Alaska — —
Not listed Phoenix Arizona — —
Not listed Long Beach California — —
Not listed Palo Alto California — —
Not listed Davenport Iowa — —
Not listed Lexington Kentucky — —
Not listed Baton Rouge Louisiana — —
Not listed Detroit Michigan — —
Not listed Minneapolis Minnesota — —
Not listed Kansas City Missouri — —
Not listed Raleigh North Carolina — —
Not listed Mayfield Heights Ohio — —
Not listed Wynnewood Pennsylvania — —
Not listed Spartanburg South Carolina — —
Not listed Kingsport Tennessee — —
Not listed Memphis Tennessee — —
Not listed Dallas Texas — —
Not listed Fort Worth Texas — —
Not listed Burlington Vermont — —

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 NCT00271544, 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 Sep 28, 2009 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00271544 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →