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ENdothelial Healing Assessment With Novel Coronary tEchnology

NCT02747199 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 13

Last updated 2017-05-04

No results posted yet for this study

Summary

This is a prospective, non-randomized, single center clinical trial to assess neointimal coverage on the stent or scaffold strut and apposition of SYNERGY™ and ABSORB in minimum of 12 eligible human subject at 4 month and 12 month after stent or scaffold implantation using OCT and CAS

Conditions

Interventions

DEVICE

SYNERGY stent

DEVICE

BVS ABSORB scaffold

Sponsors & Collaborators

  • Boston Scientific Corporation

    collaborator INDUSTRY

  • Kurume University

    collaborator OTHER

  • University of Malaya

    lead OTHER

Principal Investigators

  • Wan Azman Wan Ahmad · University Malaya Medical Center

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-08-31
Primary Completion
2016-07-31
Completion
2017-04-12

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Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02747199 on ClinicalTrials.gov