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NCT00763698 · ClinicalTrials.gov registry record · NA

Safety and Efficacy Study of the QuickFlex Micro Model 1258T Left Heart Pacing Lead

A NA study, sponsored by Abbott Medical Devices.

Completed
Registry status
NA
Development phase
86
Enrollment target

NCT00763698: Completed NA study, sponsored by Abbott Medical Devices.

NCT00763698 is a NA study that has completed, run by Abbott Medical Devices. The registered enrollment target is 86 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00763698, a NA study, has completed, sponsored by Abbott Medical Devices.

COMPLETED
Registry status
NA
Development phase
86 participants
Enrollment target

Study Summary

This is a prospective, multi-center non-randomized clinical study to evaluate the safety and efficacy of the QuickFlex Micro Model 1258T left ventricular lead in a heart failure patient population. The study will be conducted at a maximum of 20 investigational centers located in the United States and a total of 68 patients will be enrolled.

Primary Outcome

A Kaplan-Meier survival analysis was carried out for left ventricular lead related complications through 3 months. Percentage of patients who remained free from complications at 3 months was reported.

Interventions

  • DEVICE QuickFlex Micro Model 1258T Left Heart Lead

Trial Details

FieldValue
Enrollment Target 86 participants
Start Date 2008-10
Est. Completion 2010-05
Phase NA
Abbott Medical Devices

261 total trials

What the finished NCT00763698 record still lists

NCT00763698 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 86 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 1 intervention - of which QuickFlex Micro Model 1258T Left Heart Lead is the first listed.

NCT00763698 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00763698 about?

NCT00763698 is a clinical study titled "Safety and Efficacy Study of the QuickFlex Micro Model 1258T Left Heart Pacing Lead". This is a prospective, multi-center non-randomized clinical study to evaluate the safety and efficacy of the QuickFlex Micro Model 1258T left ventricular lead in a heart failure patient population. The study will be conducted at a maximum of 20 investigational centers located in the United States an...

What is the current status of trial NCT00763698?

This trial is currently completed. It is a NA study. The enrollment target is 86 participants. The study started on 2008-10. Estimated completion is 2010-05.

What interventions are being tested in trial NCT00763698?

The interventions under investigation include: QuickFlex Micro Model 1258T Left Heart Lead (DEVICE).

Who is sponsoring clinical trial NCT00763698?

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 NCT00763698's enrollment target sits among peer trials

86 976th of 2000 higher than 1,021 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 NCT00763698, the US trial registry maintained by the National Library of Medicine. NCT00763698 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.