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NCT00340509

A Genome-Wide Scan For Quantitative Trait Loci of Serum Bilirubin - A Framingham Study

Completed Last updated 16 December 2019
What this trial tests

trial in Genetics in 1,888 participants. Completed in 23 July 2013.

Timeline
26 October 2001
23 July 2013

Quick facts

Lead sponsorNational Heart, Lung, and Blood Institute (NHLBI)
StatusCompleted
Study typeOBSERVATIONAL
Enrollment1,888
Start date26 October 2001
Estimated completion23 July 2013
Sites1 location across United States

Conditions studied

Sponsor

National Heart, Lung, and Blood Institute (NHLBI)

Who can join

Eligibility, any sex, with Genetics. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Studies have shown that there is a significant association between serum bilirubin concentrations and risk of coronary artery disease (CAD). So far, no linkage analysis in humans between serum bilirubin and DNA markers has been reported. The purpose of this protocol is to identify chromosome regions that contain quantitative trait loci (QTL) involved in serum bilirubin metabolism and bilirubin concentration. In the Framingham Study, a 10cM genome scan (about 400 markers) has been conducted in more than three hundred families. Serum bilirubin was measured in the first and second exams of the Framingham Offspring. These data provide us the opportunity to undertake linkage analyses to map QTL of serum bilirubin.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Genetics

Currently open trials in the same condition.

Other National Heart, Lung, and Blood Institute (NHLBI) trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00340509.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing