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Impact of evolocumab on periprocedural microvascular damage in patients undergoing percutaneous coronary intervention (PCI)

Impact of evolocumab on periprocedural microvascular damage in patients undergoing percutaneous coronary intervention (PCI) - EVOLUTION Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000031990
Enrollment
100
Registered
2018-03-29
Start date
2018-04-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

stable coronary artery disease

Interventions

Evolocumab standard of care

Sponsors

Hyogo College of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients aged 20 to 85 years at the time of informed consent. (2) Patients with stable coronary artery disease who are planned to undergo PCI. (3) Patients with high LDL-C levels after at least 2-week treatment of high-dose statin (4) Patients who are capable of providing written consent.

Exclusion criteria

Exclusion criteria: (1) Any prior use of PCSK9 inhibitor therapy. (2) Patients with previous MI in the terriory of the target coronary artery. (3) Patients with target vessels which are two, three, or LMT. (4) Patients with recent MI in past 6 weeks (5) Patients with heart failure of New York Heart Failure Association class III or IV (6) Patients with last known left ventricular ejection fraction <30%. (7) Patients with serious renal impairment with an eGFR <30 mL/min/1.73 m2 at screening (8) Patients with hepatic dysfunction with AST or ALT 3-fold of upper limit of normal (ULN) at screening (9) Patients who are pregnant, possibly pregnant, or breast feeding. (10) Patients who have been enrolled in other clinical studies at the same time with this study (excluding observational studies such as registry studies). (11) Patients who are judged by the investigator or subinvestigators to be not suitable for participation in the study.

Design outcomes

Primary

MeasureTime frame
Index of microvascular resistance after PCI

Countries

Japan

Contacts

Public ContactMasanori Asakura

Hyogo College of Medicine Internal Medicine, Cardiovascular Division

ma-asakura@hyo-med.ac.jp0798-45-6553

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026