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NCT00305214 · ClinicalTrials.gov registry record · NA

MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post MI Patients

A NA study, sponsored by Medtronic Cardiac Rhythm and Heart Failure.

Completed
Registry status
NA
Development phase
405
Enrollment target

NCT00305214: Completed NA study, sponsored by Medtronic Cardiac Rhythm and Heart Failure.

NCT00305214 is a NA study that has completed, run by Medtronic Cardiac Rhythm and Heart Failure. The registered enrollment target is 405 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (71% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00305214, a NA study, has completed, sponsored by Medtronic Cardiac Rhythm and Heart Failure.

COMPLETED
Registry status
NA
Development phase
405 participants
Enrollment target

Study Summary

The purpose of the study is to determine the usefulness of Microvolt T Wave Alternans (MTWA) testing of patients that have had a heart attack and have decreased pumping ability of the lower chamber of their heart. MTWA testing is a non-invasive test used to detect the likelihood of developing abnormally fast rhythms in the lower chambers of the heart. The objective of the study is to prove that if a patient has a positive MTWA test, they will be more likely to develop abnormally fast and dangerous rhythms in the lower chambers of the heart. The results of the study will help doctors to determine which patients would benefit the most from having an Implantable Cardioverter Defibrillator (ICD) implanted.

Interventions

  • PROCEDURE T Wave Alternans Test

Trial Details

FieldValue
Enrollment Target 405 participants
Start Date 2003-10
Est. Completion 2007-02
Phase NA

What the finished NCT00305214 record still lists

NCT00305214 is an interventional study that assigns participants to a tested intervention. The registered 405 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (71% lower).

The record links to 0 conditions, and to 1 intervention - of which T Wave Alternans Test is the first listed.

NCT00305214 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00305214 about?

NCT00305214 is a clinical study titled "MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post MI Patients". The purpose of the study is to determine the usefulness of Microvolt T Wave Alternans (MTWA) testing of patients that have had a heart attack and have decreased pumping ability of the lower chamber of their heart. MTWA testing is a non-invasive test used to detect the likelihood of developing abnorm...

What is the current status of trial NCT00305214?

This trial is currently completed. It is a NA study. The enrollment target is 405 participants. The study started on 2003-10. Estimated completion is 2007-02.

What interventions are being tested in trial NCT00305214?

The interventions under investigation include: T Wave Alternans Test (PROCEDURE).

Who is sponsoring clinical trial NCT00305214?

This trial is sponsored by Medtronic Cardiac Rhythm and Heart Failure, which has 115 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00305214's enrollment target sits among peer trials

405 243rd of 2000 higher than 1,757 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00305214, the US trial registry maintained by the National Library of Medicine. NCT00305214 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.