Clinical trial

Safety and Efficacy of Express LD to Treat Stenosed or Occlusive Atherosclerotic…

NCT00352222 · Boston Scientific Corporation, Industry · Completed

Key facts

NCT number NCT00352222
Title Safety and Efficacy of Express LD to Treat Stenosed or Occlusive Atherosclerotic Disease in Iliac Arteries
Official title A Prospective, Multicenter, Single Arm Study to Obtain Additional Data on the Safety and Efficacy of the Express Vascular LD Implantation in the Treatment of Stenosed or Occlusive Atherosclerotic Disease in Iliac Arteries
Acronym MELODIE
Lead sponsor Boston Scientific Corporation, Industry
Collaborators KIKA
Status Completed
Phase Phase 3
Study type Interventional
Conditions Arterial Occlusive Disease, Intermittent Claudication, Atherosclerotic Disease, Thrombosis
Intervention type Device
Interventions stent implantation
Enrollment 150
Start date Jan 1, 2004
Primary completion Jul 1, 2005
Completion Feb 1, 2007
First posted Jul 14, 2006
Last update posted Sep 29, 2008
Countries Belgium, Canada, Czechia, Netherlands, Poland

At a glance

  • 10–99 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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