A Study to Compare WATCHMAN FLX Versus NOAC to Manage Embolism in Patients with Non-Valvular Atrial Fibrillation

Overview

About this study

The primary objective of this study is to determine if left atrial appendage closure with the WATCHMAN FLX device is a reasonable alternative to non-vitamin K oral anticoagulants (NOACs) in patients with non-valvular atrial fibrillation.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • The subject is of legal age to participate in the study per the laws of their respective geography.
  • The subject has documented non-valvular atrial fibrillation (i.e., atrial fibrillation in the absence of moderate or greater mitral stenosis or a mechanical heart valve).
  • The subject has a calculated CHA2DS2-VASc score of 2 or greater for men and 3 or greater for women.
  • The subject is deemed to be suitable for the protocol defined pharmacologic regimens in both the test and control arms.
  • The subject or legal representative is able to understand and willing to provide written informed consent to participate in the trial.
  • The subject is able and willing to return for required follow-up visits and examinations.

Exclusion Criteria:

  • Subjects who are currently enrolled in another investigational study, except when the subject is participating in a mandatory governmental registry, or a purely observational registry with no associated treatments.
  • The subject requires long-term anticoagulation therapy for reasons other than AFrelated stroke risk reduction, for example due to an underlying hypercoagulable state (i.e., even if the device is implanted, the subjects would not be eligible to discontinue.
  • OAC due to other medical conditions requiring chronic OAC therapy).
  • The subject is contraindicated or allergic to oral anticoagulation medication and/or aspirin.
  • The subject is indicated for chronic P2Y12 platelet inhibitor therapy.
  • The subject had or is planning to have any cardiac or non-cardiac intervention or surgical procedure within 30 days prior to or 60 days after implant (including, but not limited to: cardioversion, percutaneous coronary intervention (PCI), cardiac ablation, cataract surgery, etc.).
  • The subject had a prior stroke (of any cause, whether ischemic or hemorrhagic) or transient ischemic attack (TIA) within the 30 days prior to enrollment.
  • The subject had a prior major bleeding event per ISTH definition within the 30 days prior to randomization. Lack of resolution of related clinical sequelae or planned and pending interventions to resolve bleeding/bleeding source, are a further exclusion regardless of timing of the bleeding event.
  • The subject has an active bleed.
  • The subject has a reversible cause of AF or transient AF.
  • The subject is absent of a LAA or the LAA is surgically ligated.
  • The subject has had a myocardial infarction (MI) documented in the clinical record as either a non-ST elevation MI (NSTEMI) or as an ST-elevation MI (STEMI), with or without intervention, within 30 days prior to enrollment.
  • The subject has a history of atrial septal repair or has an ASD/PFO device.
  • The subject has an implanted mechanical valve prosthesis in any position.
  • The subject has a known contraindication to percutaneous catheterization procedure.
  • The subject has a known contraindication to TEE.
  • The subject has a cardiac tumor.
  • The subject has signs/symptoms of acute or chronic pericarditis..
  • The subject has an active infection.
  • There is evidence of tamponade physiology.
  • The subject has New York Heart Association Class IV Congestive Heart Failure at the time of enrollment.
  • The subject is of childbearing potential and is, or plans to become, pregnant during the time of the study (method of assessment upon study physician’s discretion).
  • The subject has a documented life expectancy of less than 3 years.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Mohamad Adnan Alkhouli, M.D.

Open for enrollment

Contact information:

Structural Heart Disease Research Coordinators

(507) 255-6133

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

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CLS-20511053

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