Observational Study of OCT in a Patients Undergoing FFR
Public ClinicalTrials.gov record NCT01663896. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Observational Study of Optical Coherence Tomography (OCT) in Patients Undergoing Fractional Flow Reserve (FFR) and Percutaneous Coronary Intervention Stage I (ILUMIEN I)
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The purpose of this study is to define and evaluate optical coherence tomography (OCT) stent guidance parameters through prospective data collection in percutaneous coronary intervention (PCI) procedures of de novo lesions.
Study identification
- NCT ID
- NCT01663896
- Recruitment status
- Completed
- Study type
- Observational
- Phase
- Not listed
- Enrollment
- 418 participants
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Dec 11, 2012 (Actual)
- Primary completion
- Mar 12, 2015 (Actual)
- Completion
- Oct 2015 (Actual)
- Last update posted
- Jul 2, 2020
2012 – 2015
United States locations
- U.S. sites
- 15
- U.S. states
- 12
- U.S. cities
- 15
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| University Hospital - Univ. of Alabama at Birmingham (UAB) | Birmingham | Alabama | 35233 | — |
| Scripps Clinic, Green Hospital | La Jolla | California | — | — |
| Florida Hospital Orlando | Orlando | Florida | — | — |
| Emory University Hospital | Atlanta | Georgia | — | — |
| Loyola University Chicago | Maywood | Illinois | 60153 | — |
| Central Baptist Hospital | Lexington | Kentucky | — | — |
| Baptist Health East | Louisville | Kentucky | — | — |
| St. Luke's Hospital/Mid America Heart | Kansas City | Missouri | — | — |
| Rutgers Cardiovascular Institute | New Brunswick | New Jersey | — | — |
| Mount Sinai Medical Center | New York | New York | — | — |
| Heart Hospital of Austin | Austin | Texas | — | — |
| Dallas VA Medical Center | Dallas | Texas | — | — |
| University of Texas Medical Branch at Galveston | Galveston | Texas | — | — |
| Swedish Medical Center | Seattle | Washington | — | — |
| Aurora St. Luke's Medical Center | Milwaukee | Wisconsin | — | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Non-U.S. locations
This page focuses on the U.S. directory. The official record also lists 21 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT01663896, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Jul 2, 2020 · Synced Oct 22, 2026
Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.
Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT01663896 live on ClinicalTrials.gov.