The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Renal Stent to Treat Renal Artery Stenosis

NACompletedINTERVENTIONAL
Enrollment

202

Participants

Timeline

Start Date

August 31, 2007

Primary Completion Date

June 30, 2010

Study Completion Date

December 31, 2012

Conditions
Renal Artery ObstructionHypertension, Renal
Interventions
DEVICE

Herculink Elite Renal Stent System

This is a prospective, non-randomized, single arm, multi-center study to evaluate the safety and effectiveness of the RX Herculink Elite Renal Stent System in patients with sub-optimal renal PTA results in de novo or restenotic renal artery lesions. Patients who satisfy the inclusion/exclusion criteria will be enrolled at sites in the United States. Patients will have follow up visits for evaluation.

Trial Locations (1)

95054

Abbott Vascular, Santa Clara

Sponsors
All Listed Sponsors
lead

Abbott Medical Devices

INDUSTRY