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NCT02224755 · ClinicalTrials.gov registry record · NA

MOMENTUM 3 IDE Clinical Study Protocol

A NA study, sponsored by Abbott Medical Devices.

Completed
Registry status
NA
Development phase
1,028
Enrollment target

NCT02224755: Completed NA study, sponsored by Abbott Medical Devices.

NCT02224755 is a NA study that has completed, run by Abbott Medical Devices. The registered enrollment target is 1,028 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (27% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02224755, a NA study, has completed, sponsored by Abbott Medical Devices.

COMPLETED
Registry status
NA
Development phase
1,028 participants
Enrollment target

Study Summary

The objective of the study is to evaluate the safety and effectiveness of the HM3 LVAS by demonstrating non-inferiority to the HMII LVAS (HMII) when used for the treatment of advanced, refractory, left ventricular heart failure.

Primary Outcome

Survival at 6 months free of disabling stroke (Modified Rankin Score \> 3) or reoperation to replace or remove a malfunctioning device

Interventions

  • DEVICE HeartMate 3 LVAS
  • DEVICE HeartMate II LVAS

Trial Details

FieldValue
Enrollment Target 1,028 participants
Start Date 2014-09-02
Est. Completion 2019-03-26
Phase NA
Abbott Medical Devices

261 total trials

What the finished NCT02224755 record still lists

NCT02224755 is an interventional study that assigns participants to a tested intervention. Its 1,028 participants enrollment target places it among the larger protocols in the corpus, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (27% lower).

The record links to 0 conditions, and to 2 interventions - of which HeartMate 3 LVAS is the first listed.

NCT02224755 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02224755 about?

NCT02224755 is a clinical study titled "MOMENTUM 3 IDE Clinical Study Protocol". The objective of the study is to evaluate the safety and effectiveness of the HM3 LVAS by demonstrating non-inferiority to the HMII LVAS (HMII) when used for the treatment of advanced, refractory, left ventricular heart failure.

What is the current status of trial NCT02224755?

This trial is currently completed. It is a NA study. The enrollment target is 1,028 participants. The study started on 2014-09-02. Estimated completion is 2019-03-26.

What interventions are being tested in trial NCT02224755?

The interventions under investigation include: HeartMate 3 LVAS (DEVICE), HeartMate II LVAS (DEVICE).

Who is sponsoring clinical trial NCT02224755?

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 NCT02224755's enrollment target sits among peer trials

1,028 104th of 2000 higher than 1,897 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 NCT02224755, the US trial registry maintained by the National Library of Medicine. NCT02224755 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.