Impact of Serial OCT findings After Nobori Stenting in Japanese Patients

Impact of Serial OCT findings After Nobori Stenting in Japanese Patients - Impact of Serial OCT findings After Nobori Stenting

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000008059

Enrollment

Registered

2012-05-30

Start date

2012-05-01

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

angina pectoris

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1)Older than 20 years old. (2)Indication of PCI. (3)To agree to review and record all the clinical course in this research protocol. (4)The patient who are eligible to receive dual antiplatelet therapy at least more than 6 month. (5)Informed concent with the document signed by the patients. The patient have to correspond to all the above items at the time of registration.

Exclusion criteria

Exclusion criteria: 1.The patient who died during the research 2.The patient with Stent thrombosis during the research. 3.Previous history of pancytopenia, liver function, renal dysfunction, hypersensitive history of the drug. 4.Low ejection fraction (LVEF<=30%), an impaired liver function, and renal dysfunction (eGFR<=30) 5.The patient excluded from a safety of a thiazolidine derivative. lesion exclusion criteria 1.left main artery 2.severe calcification 3.stent restenosis

Design outcomes

Primary

Measure	Time frame
To solve the percentage of neointimal coverage after Nobori stent implantation by using OCT	—

Countries

Japan

Outcome results