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Mainz Intracoronary Database. The Coronary Slow-flow and Microvascular Diseases Registry (MICAT)

J

Johannes Gutenberg University (JGU)

Status

Enrolling

Conditions

Microvascular Dysfunction
Coronary Artery Disease

Treatments

Other: observational only- no intervention

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full 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).

Enrollment

1,000 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • clinical indication to coronary angiography

Exclusion criteria

  • none

Trial design

1,000 participants in 1 patient group

Consecutive patients undergoing coronary angiography
Description:
Consecutive patients undergoing coronary angiography at the University Medical Center Mainz - no inclusion criteria specified. The absorb substudy will include consecutive patients who received an Absorb scaffold based on clinical indication.
Treatment:
Other: observational only- no intervention

Trial contacts and locations

1

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Central trial contact

Tommaso Gori, PhD, Dott medicina e Chirurgia

Data sourced from clinicaltrials.gov

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