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NCT02213484
Micro RNAs as a Marker of Aortic Aneurysm in Hereditary Aortopathy Syndromes
trial in Marfan Syndrome in 20 participants. Completed in 1 July 2016.
1 July 2016
Quick facts
| Lead sponsor | University of Colorado, Denver |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 20 |
| Start date | 1 July 2014 |
| Primary completion | 1 July 2016 |
| Estimated completion | 1 July 2016 |
| Sites | 2 locations across United States |
Conditions studied
- Marfan Syndrome — all drugs for Marfan Syndrome →
- Loeys-Dietz Syndrome — all drugs for Loeys-Dietz Syndrome →
- Thoracic Aortic Aneurysm and Dissection Syndromes — all drugs for Thoracic Aortic Aneurysm and Dissection Syndromes →
- Ehlers-Danlos Type IV Syndrome — all drugs for Ehlers-Danlos Type IV Syndrome →
Sponsor
University of Colorado, Denver
Who can join
Adults 30 Days to 60, any sex, with Marfan Syndrome or Loeys-Dietz Syndrome. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The primary objective of this study is to determine whether specific patterns of circulating micro-ribonucleic acids (miRNAs) are associated with aortic aneurysm and dissection in patients with hereditary aortopathy syndromes. The most common of these syndromes is Marfan Syndrome (MFS), but several other recognized aortopathy syndromes are well characterized. The investigators propose the use of a simple blood test, from which miRNA profiles can be measured in individuals with aortopathy syndromes to be compared with miRNAs observed in a control population that has no known predisposition for aortic disease. The investigators hypothesize that microRNA profiles in individuals with Marfan syndrome, and related disorders, will be distinct from those seen in a control group. The investigators predict that up- or down-regulation of certain miRNAs will correlate with the presence and severity of aortic aneurysm, responses to medical therapy, and ultimately could be used to determine when an individual may be at risk of dissection.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
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Novel epigenetic-based therapies useful in cardiovascular medicine.
Napoli C, Grimaldi V, De Pascale MR, Sommese L, et al · · 2016 · cited 34× · PMID 26981216 · DOI 10.4330/wjc.v8.i2.211
Verify or expand the search:
- PubMed search for NCT02213484
- Europe PMC full search
- ASCO Meeting Library
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Related trials
Other recruiting trials for Marfan Syndrome
Currently open trials in the same condition.
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- NCT04970459 — Biological Collection for Marfan and Related Syndromes · recruiting
- NCT03440697 — Pathogenetic Basis of Aortopathy and Aortic Valve Disease · active not recruiting
Other University of Colorado, Denver trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02213484 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Colorado, Denver
- Last refreshed: 15 March 2017
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/NCT02213484.
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