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Evocation Trial

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

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs051180022
Enrollment
100
Registered
2019-01-10
Start date
2019-03-22
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

[Interventional treatment] Evolocumab 140mg Q2W in addition to standard of care treatment [Standard of care treatment] Statins with/without drugs for hyperlipidemia including Ezetimib other than PCSK9

Sponsors

Ishihara Masaharu
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Patients aged 20 to 85 years. (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/1.73m2 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

Secondary

MeasureTime frame
(1) Troponin T Level (Post-PCI) (2)Change in Troponin T Level from Pre-PCI to Post-PCI (3)Change in hs-CRP Level from Pre-PCI to Post-PCI (4)Change in IL-6 Level from Pre-PCI to Post-PCI (5)Change in PTX3 Level from Pre-PCI to Post-PCI (6)Change in LOX-1 Level from Pre-PCI to Post-PCI (7) LDL-C Level (Baseline, Pre-PCI) (8)HDL-C Level (Baseline, Pre-PCI) (9)Lp(a) Level (Baseline, Pre-PCI) (10)hs-CRP Level (Baseline, Pre-PCI) (11)IL-6 Level (Baseline, Pre-PCI) (12)PTX3 Level (Baseline, Pre-PCI) (13)LOX-1 Level (Baseline, Pre-PCI) (14)BNP Level (Baseline, Pre-PCI) (15)Perioperative myocardial infarction (Post-PCI) (16)Perioperative myocardial damage (Post-PCI)

Contacts

Public ContactMasanori Asakura

Hyogo College of Medicine College Hospital

ma-asakura@hyo-med.ac.jp+81-798-45-6553

Outcome results

None listed

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