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Characterization of Interventricular Conduction Measurements

Characterization of Interventricular Conduction Measurements

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01362465
Acronym
ICM
Enrollment
25
Registered
2011-05-30
Start date
2011-06-30
Completion date
2012-04-30
Last updated
2012-09-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Brief summary

This study is an effort to use left ventricular (LV) lead based measurements to identify late electrical activation and avoid scar.

Detailed description

The aim of this study is to characterize how right ventricular (RV) to left ventricular (LV) conduction delays are altered by pacing site in patients with a cardiac resynchronization therapy (CRT) system. The study will be performed in conjunction with a CRT implant.

Interventions

PROCEDURECardiac Resynchronization Therapy

Implanting device to measure delays between paced chambers in heart failure patients.

Sponsors

Medtronic
CollaboratorINDUSTRY
Medtronic Cardiac Rhythm and Heart Failure
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient is greater than 18 years of age. * The patient or the patient's legally authorized representative is willing to give informed consent. * CRT indicated guidelines. * Patient is receiving a Medtronic IPG or ICD.

Exclusion criteria

* Patients who are pregnant. * Patient is in AF. * Patient with 3rd degree AV block.

Design outcomes

Primary

MeasureTime frameDescription
Measure how RV to LV conduction times are altered by pacing site in patients with a CRT system.30 minutesThis procedure will take approximately 30 minutes prior to implant of a CRT system. At completion of this study the patient is not followed and will be transferred to another study if enrolled in a clinical or followed as a routine implant by the center.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026