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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03172507
Other study ID # NL58806.091.16
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 20, 2017
Est. completion date October 1, 2018

Study information

Verified date October 2018
Source Radboud University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

An observational pilot proof-of-principle study. 15 patients with significant coronary artery disease and 15 matched controls. To investigate whether long-term activation of the innate immune system, named 'trained innate immunity', occurs at the level of the bone marrow progenitor cells in patients with significant coronary artery disease and whether this correlates with the proinflammatory phenotype of monocytes.


Recruitment information / eligibility

Status Completed
Enrollment 27
Est. completion date October 1, 2018
Est. primary completion date August 31, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Age =18 and =75 years

- With or without significant coronary artery disease on CCTA

- Written informed consent

Exclusion Criteria:

- Chronic infections

- Diabetes mellitus

- Medical history of any disease associated with immune deficiency

- Clinically significant infections within 3 months prior to study entry

- Recent hospital admission or surgery with general anaesthesia

- Known chronic kidney or liver disease

- Previous vaccination within 3 months prior to study entry

- Inability to personally provide written informed consent

- Inability to undergo PET-CT scanning

- Chronic use of anti-inflammatory drugs such as NSAIDs

- History of haematological malignant disease

- Documented bleeding diathesis or thrombocytopenia

- Pregnancy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Netherlands Department of cardiology, CWZ Nijmegen Gelderland
Netherlands Department of cardiology, Radboudumc Nijmegen Gelderland

Sponsors (2)

Lead Sponsor Collaborator
Radboud University Canisius-Wilhelmina Hospital

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Phenotypical characteristics of HSPC's Phenotypical characteristics of HSPC's populations of patients with and without significant coronary artery disease by flowcytometry in percentages. Study day 2 for patients
Primary Cytokine response of circulating monocytes Cytokine response of monocytes of patients with and without significant coronary artery disease after 24 hour stimulation with several stimuli measured in cytokine levels. Study day 2 for patients
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