Pilot Study of the Fantom Bioresorbable Scaffold (FANTOM I)
NCT02512003 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 7
Last updated 2023-03-29
Summary
The FANTOM I pilot study is intended to assess safety of the Fantom Bioresorbable Coronary Scaffold in native coronary arteries.
Conditions
Interventions
- DEVICE
-
Fantom Scaffold
Sponsors & Collaborators
-
REVA Medical, Inc.
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-12-31
- Primary Completion
- 2015-07-31
- Completion
- 2020-04-30
Countries
- Brazil
- Poland
Study Locations
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