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REPARA Study: REgistry of PAtients With bioResorbable Device in Daily Clinical prActice

NCT02256449 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 2440

Last updated 2016-07-18

No results posted yet for this study

Summary

A multicentre, observational, prospective device registry, with no control group, designed to evaluate the efficacy and safety of the bioresorbable coronary device, used according to the indications of use, in daily clinical practice in a consecutive number of patients undergoing PCI in de novo coronary artery lesions. A total of 1,500 patients are planned to be included in the registry.

Conditions

  • Coronary Artery Lesions With Implantation of Coronary Device

Sponsors & Collaborators

  • Sección Hemodinamica y Cardiologia Intervencionista

    lead OTHER

Principal Investigators

  • Felipe Hernandez, MD · Seccion Hemodinamica y Cardiologia Intervencionista

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2015-09-30
Completion
2016-10-31

Countries

  • Spain

Study Locations

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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 NCT02256449 on ClinicalTrials.gov