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NCT03688815 Clinical Trial

Dipyridamole Induced Ischemia and Biomarkers

Ischemic Heart Disease Clinical Trial

Official title:
Relationship Between the L-arginine Pathway Metabolites and Dipyridamole Stress Induced Transient Myocardial Ischaemia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03688815
Other study ID # PTE3950
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2009
Est. completion date January 1, 2017

Study information
Verified date September 2018
Source University of Pecs
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Analysis of certain biomarkers and transient myocardial perfusion deficit revealed by myocardial perfusion scintigraphy.

Description:

The prospectively enrolled patients were followed up to 5 years. Adverse major events (MI, stroke, death) suffered during follow-up were retrospectively analysed.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date January 1, 2017
Est. primary completion date January 1, 2010
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1. written informed consent. 2. clinical diagnosis of ischemic heart disease (IHD) -

Exclusion Criteria: 1. refused written informed consent. 2. lost data during follow-up

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• myocardial perfusion scintigraphy
Myocardial perfusion scintigraphy as it is described in the international literature.

Locations
Country Name City State
Hungary University of Pecs Pécs Baranya

Sponsors (1)
Lead Sponsor Collaborator
University of Pecs

Country where clinical trial is conducted

Hungary, 

Outcome
Type Measure Description Time frame Safety issue
Primary Myocardial perfusion abnormality Myocardial perfusion was quantified based on myocardial perfusion scintigraphy (MPS). 5 year follow-up after MPS
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