Optimization of Cardiac Pacing Using CardioMEMS

NCT ID: NCT03581032

Last Updated: 2018-07-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-03-01

Study Completion Date

2019-06-01

Brief Summary

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This study is designed to determine if a simplified technique for cardiac device reprogramming using pulmonary artery pressure (PAP) data in the acute setting holds promise to improve subjective assessments of patient quality of life (QOL), objective measurements of functional capacity, and specific systolic and diastolic echocardiographic indices.

Detailed Description

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The present study is designed to determine if a simplified technique for cardiac device( CRT) reprogramming using pulmonary artery pressure (PAP) via implanted CardioMEMS device data in the acute setting holds promise to improve subjective assessments of patient quality of life (QOL), objective measurements of functional capacity, and specific systolic and diastolic echocardiographic indices. The protocol requires prospective collection and analysis of echocardiographic data, subjective symptoms (Minnesota Living with Heart Failure Questionnaires), and 6-minute walk distance measurements in patients with implanted biventricular pacemakers / defibrillators who are predominantly ventricularly paced, in normal sinus rhythm, have documented NYHA class 3 Heart Failure, and have implanted pulmonary artery pressure monitors (CardioMEMS, St. Jude Medical CRMD, St. Paul, MN). Data collection will occur at presentation (rest and with ambulation), one month post-reprogramming, and two months after evaluation and / or reprogramming.

Conditions

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Heart Failure

Study Design

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Observational Model Type

CASE_CROSSOVER

Study Time Perspective

PROSPECTIVE

Study Groups

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A-Active reprogram follwed by sham

This arm will be randomized to have PACING device reprogramming followed by sham reprogramming

Active reprogam

Intervention Type DEVICE

Reprogram Changes in AV/PV delays

B-Sham followed by active reprogram

This arm will be randomized to have sham reprogramming followed by active pacing reprogramming

Active reprogam

Intervention Type DEVICE

Reprogram Changes in AV/PV delays

Interventions

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Active reprogam

Reprogram Changes in AV/PV delays

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Patients have implanted PPM, ICD, or CRT devices and CardioMEMS
2. Patients can ambulate for 6 minutes and lay on a flat surface
3. Patients are paced \> 95% of the time
4. Patients are not in acute CHF and are on a stable medication regimen
5. Patients have adequate echocardiographic windows
6. Patients can consent independently

Exclusion Criteria

1. Patients with poor echocardiographic acoustical resolution.
2. Patients with congenital heart disease.
3. Patients with mechanical aortic or mitral valve replacements.
4. Patients with significant mitral annular calcification.
5. Patients with irregular heart rates: atrial fibrillation, supraventricular tachycardia, atrial premature contractions, and ventricular arrhythmia that would preclude data acquisition.
6. Patients unable to remain still secondary to movement disorders or agitation.
7. Inpatient status
8. Patients with poorly controlled HTN (SBP\>160/90
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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St. Francis Hospital, New York

OTHER

Sponsor Role lead

Responsible Party

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Rita Jermyn, MD

Director of Center for Cardiac Therapeutics

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Rita Jermyn, MD

Role: PRINCIPAL_INVESTIGATOR

Saint Francis Hospital

Locations

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St Francis Hospital

Roslyn, New York, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Elizabeth S Haag, BSN MPA

Role: CONTACT

516 622-4512

Rita Jermyn, MD

Role: CONTACT

516 562-6426

Facility Contacts

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Elizabeth Haag, BSN MPA

Role: primary

516-622-4512

Rita Jermyn, MD

Role: backup

516 562-6646

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Other Identifiers

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17-13

Identifier Type: -

Identifier Source: org_study_id

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