NIPH Clinical Trials Search

JAPANESE
JRCT ID: jRCT1040250123

Registered date:29/10/2025

The Hokuriku-plus Acute Coronary Syndrome Registry Study

Basic Information

Recruitment status Recruiting
Health condition(s) or Problem(s) studiedAcute coronary syndrome
Date of first enrollment29/10/2025
Target sample size1000
Countries of recruitment
Study typeInterventional
Intervention(s)Implement LDL cholesterol management using a standardized clinical pathway and conduct familial hypercholesterolemia screening, considering genetic testing as needed.

Outcome(s)

Primary OutcomeAchievement of LDL cholesterol management target (<55 mg/dL) at 4 weeks.
Secondary OutcomeAchievement of LDL cholesterol management target (< 55 mg/dL) at 12 weeks and 52 weeks. Achievement of LDL cholesterol management target (< 70 mg/dL) at 4 weeks, 12 weeks, and 52 weeks. Presence/absence of familial hypercholesterolemia diagnosis at 52 weeks. Cardiac events, safety (adverse events).

Key inclusion & exclusion criteria

Age minimum>= 18age old
Age maximumNot applicable
GenderBoth
Include criteria1) Patients hospitalized for acute coronary syndrome 2) Age 18 years or older 3) Written informed consent obtained from the patient voluntarily after providing sufficient informed consent regarding participation in this clinical study
Exclude criteria1) Patients who find it difficult to attend regular outpatient appointments 2) Patients who are pregnant or breastfeeding 3) Other patients deemed unsuitable for the program at the physician's discretion

Related Information

Contact

Public contact
Name Yasuaki Takeji
Address 13-1 Takara-machi Kanazawa Ishikawa Ishikawa Japan 920-8641
Telephone +81-76-265-2251
E-mail takeji0622@gmail.com
Affiliation Kanazawa University Hospital
Scientific contact
Name Hayato Tada
Address 13-1 Takara-machi Kanazawa Ishikawa Ishikawa Japan 920-8641
Telephone +81-76-265-2000
E-mail ht240z@sa3.so-net.ne.jp
Affiliation Kanazawa University Hospital