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Completed Not applicable Interventional Results available

Reducing Episodes by Septal Pacing Efficacy Confirmation Trial (RESPECT)

ClinicalTrials.gov ID: NCT00289289

Public ClinicalTrials.gov record NCT00289289. 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 21, 2026, 10:37 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 purpose of this study is to find out if specialized programs in the AT500 and EnRhythm pacemakers will reduce the number of irregular heartbeat in the upper chamber of the heart and reduce symptoms (such as shortness of breath, dizziness, and others).

Study identification

NCT ID
NCT00289289
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
400 participants

Conditions and interventions

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
Feb 2004 (Type not available)
Primary completion
Nov 2010 (Actual)
Completion
Jul 2011 (Actual)
Last update posted
Aug 8, 2012

2004 – 2011

United States locations

U.S. sites
34
U.S. states
23
U.S. cities
34
Facility City State ZIP Site status
Not listed Little Rock Arkansas — —
Not listed Rancho Mirage California — —
Not listed San Diego California — —
Not listed Yuba City California — —
Not listed Colorado Springs Colorado — —
Not listed Jacksonville Florida — —
Not listed Lakeland Florida — —
Not listed Chicago Illinois — —
Not listed Decatur Illinois — —
Not listed Urbana Illinois — —
Not listed Indianapolis Indiana — —
Not listed Cedar Rapids Iowa — —
Not listed Louisville Kentucky — —
Not listed Owensboro Kentucky — —
Not listed Takoma Park Maryland — —
Not listed Springfield Massachusetts — —
Not listed Minneapolis Minnesota — —
Not listed Clifton New Jersey — —
Not listed Morristown New Jersey — —
Not listed Albuquerque New Mexico — —
Not listed Mineola New York — —
Not listed Charlotte North Carolina — —
Not listed Cleveland Ohio — —
Not listed Columbus Ohio — —
Not listed Hershey Pennsylvania — —
Not listed Spartanburg South Carolina — —
Not listed Amarillo Texas — —
Not listed Austin Texas — —
Not listed Corpus Christi Texas — —
Not listed Fort Worth Texas — —
Not listed Salt Lake City Utah — —
Not listed Burlington Vermont — —
Not listed Richmond Virginia — —
Not listed Morgantown West 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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00289289, 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 Aug 8, 2012 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00289289 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →