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Safety and efficacy of optical coherence tomography-guided XienceTM stent implantation compared with angiography-guided in patients with acute coronary syndrome; Observational Clinical Trial

Safety and efficacy of optical coherence tomography-guided XienceTM stent implantation compared with angiography-guided in patients with acute coronary syndrome; a multicenter, prospective, Observational Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0003925
Enrollment
800
Registered
2019-05-16
Start date
2018-02-28
Completion date
Unknown
Last updated
2019-05-20

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

Conditions

None listed

Interventions

None listed

Sponsors

Chonnam National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) A patient who is diagnosed with acute coronary syndrome over the age of 19 and is scheduled to have a coronary intervention treatment with a XienceTM stent. (2) A patient who decides to participate in this study voluntarily and agrees in writing to the subject's consent

Exclusion criteria

Exclusion criteria: (1) Patients who have taboo or hypersensitivity to treatment of anti-platelet (2) Patients with creatin levels greater than 2.0 mg/dL (3) If life expectancy is less than 1 year (4) A woman who is pregnant or wishes to conceive (5) Cardiopathic shock or Killip Classification IV patient

Design outcomes

Primary

MeasureTime frame
Rate of failure of target lesions (combination of cardiac death, target vascular myocardial infarction, and ischemia - induced target lesion reconstruction)—

Secondary

MeasureTime frame
Incidence of myocardial infarction after Percutaneous coronary artery intervention;Complication rate after Percutaneous coronary artery intervention;time of procedure;Total Contrast Agents;Total radiation dose—

Countries

Korea, Republic of

Contacts

Public ContactYURI KIM

Chonnam National University Hospital

kyr5006@naver.com+82-62-220-5272

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026