Comparison of the Healing response of Durable polymer versus Bioresorbable polymer DES in patients with acute coronary syndrome

Comparison of the Healing response of Durable polymer versus Bioresorbable polymer DES in patients with acute coronary syndrome - HR-ACS study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000028967

Enrollment

100

Registered

2017-09-01

Start date

2016-06-24

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

Acute coronary syndrome

Interventions

Synergy group XIENCE group

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with acute coronary syndrome more than 20 years old Informed concent

Exclusion criteria

Exclusion criteria: less than 20 years old Indication of CABG Patients need anti-cancer drug Patients need non cardiac surgery within 6M Cardiogenick shock and ADHF Patients with severe kidney D. Other reasons (not suitable for this study)

Design outcomes

Primary

Measure	Time frame
Comparison of the healing response by the OCT findings between Synergy and XIENCE after 6 monts in patients with ACS.	—

Secondary

Measure	Time frame
In staged PCI case, OCT findings also compared between two groups after 1 month of ACS-onset.	—

Countries

Japan

Contacts

Public ContactShinya Okazaki

Juntendo University School of Medicine Department of Cardiovascular Medicine

shinya@juntendo.ac.jp0333672908

Outcome results

None listed

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