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NCT03830736
Health Effects of Oats and Oat Bioactive in Human
NA trial testing Oat Beverage 1 in Postprandial Glucose Regulation in 24 participants. Completed in 30 December 2019.
30 May 2019
Quick facts
| Lead sponsor | Lund University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | single |
| Primary purpose | prevention |
| Enrollment | 24 |
| Start date | 18 February 2019 |
| Primary completion | 30 May 2019 |
| Estimated completion | 30 December 2019 |
| Sites | 1 location across Sweden |
Drugs / interventions tested
- Oat Beverage 1
- Oat Beverage 2
- Oat Beverage 3
- Oat Beverage 4
- Control product — full drug profile →
Conditions studied
- Postprandial Glucose Regulation — all drugs for Postprandial Glucose Regulation →
Sponsor
Lund University
Who can join
Adults 20 to 40, any sex, with Postprandial Glucose Regulation. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Aim of the study is to investigate health effects of oats and oat derived components, in human intervention studies, with the purpose to build new knowledge for development of cardiometabolic protective foods.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Oat Polar Lipids Improve Cardiometabolic-Related Markers after Breakfast and a Subsequent Standardized Lunch: A Randomized Crossover Study in Healthy Young Adults.
Hossain MM, Tovar J, Cloetens L, Florido MTS, et al · · 2021 · cited 10× · PMID 33803802 · DOI 10.3390/nu13030988
Verify or expand the search:
- PubMed search for NCT03830736
- 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 NCT03830736 (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 Lund University
- Last refreshed: 1 May 2020
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/NCT03830736.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing