SPIRIT II: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary Stent System
A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary Stent System in the Treatment of Patients With de Novo Native Coronary Artery Lesions
Sponsor: Abbott Medical Devices
A PHASE3 clinical study on Coronary Artery Disease and Coronary Disease, this trial is completed. The trial is conducted by Abbott Medical Devices and has accumulated 7 data snapshots since 2005. Cardiovascular trials of this type often inform treatment guidelines for long-term patient management.
Change History
7 versions recorded-
Sep 2025 — Present [monthly]
Completed PHASE3
-
Sep 2024 — Sep 2025 [monthly]
Completed PHASE3
-
Jul 2024 — Sep 2024 [monthly]
Completed PHASE3
-
Jan 2021 — Jul 2024 [monthly]
Completed PHASE3
-
Dec 2018 — Jan 2021 [monthly]
Completed PHASE3
▶ Show 2 earlier versions
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Jun 2018 — Dec 2018 [monthly]
Completed PHASE3
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Jan 2017 — Jun 2018 [monthly]
Completed PHASE3
First recorded
Jul 2005
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Abbott Medical Devices
For direct contact, visit the study record on ClinicalTrials.gov .
Study Locations
Aalborg, Denmark, Aarhus, Denmark, Amsterdam, Netherlands, Antwerp, Belgium, Auckland, New Zealand, Bad Oeynhausen, Germany, Bad Segeberg, Germany, Basel, Switzerland, Breda, Netherlands, Cape Town, South Africa and 18 more location s