Clinical trial
The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite…
NCT00490841 · Abbott Medical Devices, Industry · Completed
Key facts
| NCT number | NCT00490841 |
|---|---|
| Title | The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Renal Stent to Treat Renal Artery Stenosis |
| Official 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. |
| Acronym | HERCULES |
| Lead sponsor | Abbott Medical Devices, Industry |
| Status | Completed |
| Study type | Interventional |
| Conditions | Renal Artery Obstruction, Hypertension, Renal |
| Intervention type | Device |
| Interventions | Herculink Elite Renal Stent System |
| Enrollment | 202 |
| Start date | Aug 1, 2007 |
| Primary completion | Jun 1, 2010 |
| Completion | Dec 1, 2012 |
| First posted | Jun 25, 2007 |
| Last update posted | Dec 18, 2012 |
| Countries | United States |
At a glance
- 1–9 Study sites
- Yes Results posted
- 1–9 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: