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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01414361
Other study ID # H-1106-077-366
Secondary ID
Status Recruiting
Phase Phase 4
First received August 9, 2011
Last updated August 10, 2011
Start date March 2009
Est. completion date November 2011

Study information

Verified date August 2011
Source Seoul National University Hospital
Contact Bon-Kwon Koo, MD/PhD
Phone 82-2-2072-2062
Email bkkoo@snu.ac.kr
Is FDA regulated No
Health authority South Korea: Institutional Review Board
Study type Observational

Clinical Trial Summary

Recent studies have shown that optimal IVUS criteria defining the functional significance (FFR < 0.8) of intermediate coronary stenoses is different according to their locations of the coronary tree. Herein, the investigators performed this study to validate these results and to generalize the IVUS criteria defining functional significance of intermediate coronary stenosis in a different location of coronary tree in a larger sample size.


Description:

Both physiologic information from fractional flow reserve (FFR) and anatomical information from intravascular ultrasound (IVUS) in assessing intermediate coronary stenotic lesions are useful. Functional significance of a coronary stenosis is determined by both the severity of a stenosis and the amount of myocardium supplied. Therefore, when the functional significance of a lesion is assessed by lumen area measured by IVUS, different criteria should be applied according to lesion location and anatomical variations of the coronary artery. However, previous studies included only patients with proximal lesions or small vessel disease, and the sample sizes were too small to assess these differences. In a recent study, the investigators have shown that optimal IVUS criteria defining the functional significance (FFR < 0.8) of intermediate coronary stenoses is different according to their locations of the coronary tree. Herein, the investigators performed this study to validate the our results and to generalize the IVUS criteria defining functional significance of intermediate coronary stenosis in a different location of coronary tree in a larger sample size.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date November 2011
Est. primary completion date November 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Intermediate coronary stenosis by visual estimation

Exclusion Criteria:

- history of coronary artery bypass graft surgery

- previously revascularized lesion

- creatinine > 1.6 mg/dL or eGFR < 30 ml/min/1.73m2 pre-procedure per institutional standards

- known pregnancy

- contrast agent allergy that cannot be adequately premedicated

- severe PVD precluding cardiac catheterization

- patient not a candidate for IVUS and FFR

- inability or unwillingness to provide informed consent

- inability or unwillingness to perform required follow up procedures

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (7)

Lead Sponsor Collaborator
Seoul National University Hospital Asan Medical Center, Inje University, Keimyung University, National University, Singapore, University of Florida, Washington Hospital Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary lumen area lumen area cut-off that can predict functional significance of a lesion day 1 No
Secondary angiographic stenosis, % plaque area angiographic and intravascular ultrasound parameters that can best predict the functional significance of lesions day 1 No
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