Clinical trial design and rationale of the Multicenter Study of MagLev Technology in Patients Undergoing Mechanical Circulatory Support Therapy with HeartMate 3 (MOMENTUM 3) investigational device exemption clinical study protocol

Gerald Heatley, Poornima Sood, Daniel J. Goldstein, Nir Uriel, Joseph Cleveland, Don Middlebrook, Mandeep R. Mehra

Research output: Contribution to journalArticle

53 Citations (Scopus)

Abstract

The HeartMate 3 left ventricular assist system (LVAS; St. Jude Medical, Inc., formerly Thoratec Corporation, Pleasanton, CA) was recently introduced into clinical trials for durable circulatory support in patients with medically refractory advanced-stage heart failure. This centrifugal, fully magnetically levitated, continuous-flow pump is engineered with the intent to enhance hemocompatibility and reduce shear stress on blood elements, while also possessing intrinsic pulsatility. Although bridge-to-transplant (BTT) and destination therapy (DT) are established dichotomous indications for durable left ventricular assist device (LVAD) support, clinical practice has challenged the appropriateness of these designations. The introduction of novel LVAD technology allows for the development of clinical trial designs to keep pace with current practices. The prospective, randomized Multicenter Study of MagLev Technology in Patients Undergoing Mechanical Circulatory Support Therapy With HeartMate 3 (MOMENTUM 3) clinical trial aims to evaluate the safety and effectiveness of the HeartMate 3 LVAS by demonstrating non-inferiority to the HeartMate II LVAS (also St. Jude Medical, Inc.). The innovative trial design includes patients enrolled under a single inclusion and exclusion criteria, regardless of the intended use of the device, with outcomes ascertained in the short term (ST, at 6 months) and long term (LT, at 2 years). This adaptive trial design includes a pre-specified safety phase (n = 30) analysis. The ST cohort includes the first 294 patients and the LT cohort includes the first 366 patients for evaluation of the composite primary end-point of survival to transplant, recovery or LVAD support free of debilitating stroke (modified Rankin score >3), or re-operation to replace the pump. As part of the adaptive design, an analysis by an independent statistician will determine whether sample size adjustment is required at pre-specified times during the study. A further 662 patients will be enrolled to reach a total of 1,028 patients for evaluation of the secondary end-point of pump replacement at 2 years.

Original languageEnglish (US)
Pages (from-to)528-536
Number of pages9
JournalJournal of Heart and Lung Transplantation
Volume35
Issue number4
DOIs
StatePublished - Apr 1 2016

Fingerprint

Clinical Protocols
Multicenter Studies
Clinical Trials
Technology
Equipment and Supplies
Heart-Assist Devices
Therapeutics
Transplants
Safety
Clinical Studies
Sample Size
Heart Failure
Stroke
Survival

Keywords

  • advanced heart failure
  • HeartMate 3
  • LVAD
  • MagLev
  • MOMENTUM 3

ASJC Scopus subject areas

  • Transplantation
  • Cardiology and Cardiovascular Medicine
  • Pulmonary and Respiratory Medicine
  • Surgery

Cite this

Clinical trial design and rationale of the Multicenter Study of MagLev Technology in Patients Undergoing Mechanical Circulatory Support Therapy with HeartMate 3 (MOMENTUM 3) investigational device exemption clinical study protocol. / Heatley, Gerald; Sood, Poornima; Goldstein, Daniel J.; Uriel, Nir; Cleveland, Joseph; Middlebrook, Don; Mehra, Mandeep R.

In: Journal of Heart and Lung Transplantation, Vol. 35, No. 4, 01.04.2016, p. 528-536.

Research output: Contribution to journalArticle

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