Clinical trial
A Clinical Trial to Assess the Safety and Efficacy of the RX Herculink(R) Elite(TM) Renal Stent System for the Treatment of Suboptimal Post-procedural Percutaneous Transluminal Angioplasty (PTA) in de Novo or Restenotic Renal Artery Stenoses in Patients With Uncontrolled Hypertension.
NCT00490841 is registered in ClinicalTrials.gov with Abbott Medical Devices as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Clinical Trial to Assess the Safety and Efficacy of the RX Herculink(R) Elite(TM) Renal Stent System for the Treatment of Suboptimal Post-procedural Percutaneous Transluminal Angioplasty (PTA) in de Novo or Restenotic Renal Artery Stenoses in Patients With Uncontrolled Hypertension.
- Lead sponsor
- Abbott Medical Devices
- Phase
- Not applicable
- Overall status
- Completed
- Start date
- August 31, 2007
- Completion date
- December 31, 2012
- Enrollment
- 202 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.