QuickOptTM Study - Using the QuickOptTM Method for Timing Cycle Optimization

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

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-09-30

Study Completion Date

2009-09-30

Brief Summary

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QuickOptTM optimization method provides a quicker, simpler and reliable alternative to standard echocardiography methods for optimization of sensed AV, paced AV and V-V delays in patients with CRT-P devices

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Detailed Description

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Conditions

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Heart Failure

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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QuickOpt

QuickOpt is an optimization algorithm to program the AV, PV and VV delays

Group Type EXPERIMENTAL

QuickOpt

Intervention Type DEVICE

The QuickOpt algorithm will suggest values for programming AV, PV and VV delay.

Interventions

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QuickOpt

The QuickOpt algorithm will suggest values for programming AV, PV and VV delay.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patient meets current CRT-P indications and be implanted with an SJM CRT-P device with V-V timing and a compatible lead system
* Patient is able to provide written informed consent for study participation

Exclusion Criteria

* Patient has limited intrinsic atrial activity (≤ 40 bpm)
* Patient has persistent or permanent AF
* Patient has a 2o or 3o heart block
* Patient is unable to provide analyzable echocardiogram images
* Patient's life expectancy is \<12 months
* Patient is \<18 years old
* Patient is pregnant
* Patient is on IV inotropic agents

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No