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Clinical Trial Summary

Primary goal of the registry is to collect prospective data on patients undergoing coronary angiography in Mainz. Following amendment of the procol, this study will also include patients who received an Aborb bioresorbable scaffold for the therapy of de novo stenoses.


Clinical Trial Description

Patients included in the registry will be contacted by telephone at 3,6,9, 12 months and 2, 5, 10 years after the procedure. In case coronary slow flow is shown at the index procedure, 39ml of blood will be drawn for further studies. According to the regulations of the Province Rheinland-Pfalz, national law, and with the approval of the Ethic commission of the Landesärztekammer Rheinland Pfalz, patients (n=1000) will also be retrospectively entered in the database in an anonymous way. For these patients, no specific study procedure is foreseen and the MICAT database will be only used as a platform (database of anonymous data collected during routine clinical practice). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02180178
Study type Observational [Patient Registry]
Source Johannes Gutenberg University Mainz
Contact Tommaso Gori, PhD, Dott medicina e Chirurgia
Phone +49 6131 172829
Email tommaso.gori@unimedizin-mainz.de
Status Recruiting
Phase
Start date September 2013
Completion date September 2023

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