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NCT05661994
Omega-3 Supplementation on Serum Fetuin-A Levels
NA trial testing Omega-3 fatty acid supplementation in Coronary Artery Disease in 34 participants. Completed in 8 April 2022.
11 October 2021
Quick facts
| Lead sponsor | Amasya University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 34 |
| Start date | 18 December 2020 |
| Primary completion | 11 October 2021 |
| Estimated completion | 8 April 2022 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Omega-3 fatty acid supplementation
Conditions studied
- Coronary Artery Disease — all drugs for Coronary Artery Disease →
Sponsor
Amasya University
Who can join
Adults 35 to 75, male only, with Coronary Artery Disease. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Background and aims: One of the investigated possible modulators of serum fetuin-A, associated with the risk of developing coronary artery disease (CAD), is omega-3 fatty acids (FAs). This study aims to evaluate the effects of omega-3 FA supplementation on serum fetuin-A concentration in patients with CAD. Methods: The study was carried out on 34 male volunteer patients aged 35-75 years, newly diagnosed with CAD by conventional coronary angiography. Patients with CAD were divided into the "Omega-3 Group (n:16)" and "Control Group (n:18)". Low-fat diet principles were explained to both groups at baseline. While 1.560 mg/day omega-3 FA supplementation was given to the patients in the omega-3 group for eight weeks, but not in the control group. Food intake was recorded using six-day food records.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Effects of Omega-3 Fatty Acid Supplementation on Serum Fetuin-A Levels in Patients With Coronary Artery Disease.
Icer MA, Yıldıran H, Sahinarslan A, Topal S. · · 2025 · PMID 40538988 · DOI 10.1002/fsn3.70460
Verify or expand the search:
- PubMed search for NCT05661994
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT05661994 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 9 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 Amasya University
- Last refreshed: 22 December 2022
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/NCT05661994.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing