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OpenTrials
Completed

NCT Number: NCT02126150

United Coronary Biobanks

The UNICORN consists of two collaborating biobanks, one in Utrecht and one in Singapore. From these two sites we include all patients who undergo a coronary catheterization for any reason.

At the moment of catheterization we draw blood, which will be stored in a biobank and we collect clinical characteristics. Patients are followed-up for 5 years for the occurrence of major cardiovascular events.

By including from two sites in the world we include 4 major ethnic groups: Caucasians, Chinese, Indians and Malays. We aim at including at least 2000 patients per ethnic group.

Our hypothesis is that there are differences in the risk factor burden, clinical presentation of CAD, and biochemical patterns in the blood among the ethnic groups.

Furthermore, this biobank offers a platform for multi-ethnic biomarker discovery.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients undergoing coronary angiography

Exclusion criteria

  • < 21 years of age
  • Hemoglobin levels <7 g/dL in women, or hemoglobin levels <8 g/dL in men

Treatment and study plan

Primary outcomes

  1. All-cause death

    Time frame: 5 years

Secondary outcomes

  1. Major cardiovascular events

    Time frame: 5 years

Sponsors and collaborators

Lead sponsor

UMC Utrecht

Other

Collaborators

  • National University Hospital, Singapore

Registry information

Acronym: UNICORN

Important dates

Study start
2010
Primary completion
2015
Study completion
2015
First posted
Apr 29, 2014
Registry last updated
Dec 8, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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