Clinical trial

Evaluation of the STARFlex® Septal Closure System in Patients With a Stroke or…

NCT00201461 · NMT Medical, Industry · Unknown status

Key facts

NCT number NCT00201461
Title Evaluation of the STARFlex® Septal Closure System in Patients With a Stroke or TIA Due to the Possible Passage of a Clot of Unknown Origin Through a Patent Foramen Ovale (PFO)
Official title A Prospective, Multicenter, Randomized Controlled Trial to Evaluate the Safety and Efficacy of the STARFlex® Septal Closure System Versus Best Medical Therapy in Patients With a Stroke and/or Transient Ischemic Attack Due to Presumed Paradoxical Embolism Through a Patent Foramen Ovale
Lead sponsor NMT Medical, Industry
Status Unknown status
Phase Phase 2/Phase 3
Study type Interventional
Conditions Patent Foramen Ovale, Stroke, Ischemic Attack, Transient
Intervention type Device, Drug
Interventions STARFlex septal closure system, Best medical therapy
Enrollment 900
Start date Jun 1, 2003
Completion Apr 1, 2010
First posted Sep 20, 2005
Last update posted Dec 30, 2008
Countries United States

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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