MedTrace Logo

CRT Pilot Study for Children With Heart Failure

NCT00585065 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 7

Last updated 2023-05-11

No results posted yet for this study

Summary

To collect information on pediatric patients receiving Cardiac Resynchronization Therapy (CRT) with permanent biventricular pacing (BVP) as a method of treating chronic heart failure.

Conditions

  • Chronic Pediatric Heart Failure

Interventions

DEVICE

CRT device implant

The purpose of this study is to collect information on patients with chronic heart failure who have already been identified by their physician as candidates for CRT. All tests, including device implantation are standard of care for patients undergoing CRT. The only test involved in this study that is not standard of care is the quality of life questionnaire. Patients who undergo CRT system implant will be followed post-implant (up to 1 week), and at one month, three months, six months and twelve months. The only test involved in this study that is not standard of care is the quality of life questionnaire.

Sponsors & Collaborators

Principal Investigators

  • Elizabeth Saarel, MD · University of Utah

Eligibility

Min Age
1 Year
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-01-31
Primary Completion
2008-01-31
Completion
2016-01-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00585065 on ClinicalTrials.gov