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NCT00418314 · ClinicalTrials.gov registry record · NA

FREEDOM - A Frequent Optimization Study Using the QuickOpt Method

A NA study, sponsored by Abbott Medical Devices.

Completed
Registry status
NA
Development phase
1,647
Enrollment target

NCT00418314: Completed NA study, sponsored by Abbott Medical Devices.

NCT00418314 is a NA study that has completed, run by Abbott Medical Devices. The registered enrollment target is 1,647 participants, above the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (17% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00418314, a NA study, has completed, sponsored by Abbott Medical Devices.

COMPLETED
Registry status
NA
Development phase
1,647 participants
Enrollment target

Study Summary

The objective of this study is to demonstrate that frequent atrio-ventricular (AV/PV) and inter-ventricular (V-V) delay optimization using QuickOpt in patients with cardiac resynchronization therapy device results in improved clinical response over standard of care (i.e. empiric programming or one-time optimization using any non-intracardiac electrogram optimization methods).

Primary Outcome

The clinical composite score classifies each randomized patient as improved, unchanged, or worse depending on the clinical response during and the clinical status at the end of the trial. Patients are considered improved if at the final visit they experienced a favorable change in NYHA functional class or in the patient global assessment (or both) but did not experience any major adverse clinical events during the course of the trial. Patients are considered worse if they experienced a major cli

Interventions

  • DEVICE Control
  • DEVICE QuickOpt

Trial Details

FieldValue
Enrollment Target 1,647 participants
Start Date 2006-10
Est. Completion 2009-09
Phase NA
Abbott Medical Devices

261 total trials

What the finished NCT00418314 record still lists

NCT00418314 is an interventional study that assigns participants to a tested intervention. Its 1,647 participants enrollment target places it among the larger protocols in the corpus, above the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (17% higher).

The record links to 0 conditions, and to 2 interventions - of which Control is the first listed.

NCT00418314 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00418314 about?

NCT00418314 is a clinical study titled "FREEDOM - A Frequent Optimization Study Using the QuickOpt Method". The objective of this study is to demonstrate that frequent atrio-ventricular (AV/PV) and inter-ventricular (V-V) delay optimization using QuickOpt in patients with cardiac resynchronization therapy device results in improved clinical response over standard of care (i.e. empiric programming or one-t...

What is the current status of trial NCT00418314?

This trial is currently completed. It is a NA study. The enrollment target is 1,647 participants. The study started on 2006-10. Estimated completion is 2009-09.

What interventions are being tested in trial NCT00418314?

The interventions under investigation include: Control (DEVICE), QuickOpt (DEVICE).

Who is sponsoring clinical trial NCT00418314?

This trial is sponsored by Abbott Medical Devices, which has 261 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00418314's enrollment target sits among peer trials

1,647 63rd of 2000 higher than 1,938 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 NCT00418314, the US trial registry maintained by the National Library of Medicine. NCT00418314 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.