Last reviewed · How we verify
NCT03236259
The Effect of Berry Extract Administration on Cognitive Health
NA trial testing Brainport high dose in Cognitive Impairment in 102 participants. Completed in 21 August 2018.
21 August 2018
Quick facts
| Lead sponsor | Maastricht University Medical Center |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | prevention |
| Enrollment | 102 |
| Start date | 21 February 2017 |
| Primary completion | 21 August 2018 |
| Estimated completion | 21 August 2018 |
| Sites | 1 location across Netherlands |
Drugs / interventions tested
- Brainport high dose
- Brainport low dose
- Placebo
Conditions studied
- Cognitive Impairment — all drugs for Cognitive Impairment →
- Overweight and Obesity — all drugs for Overweight and Obesity →
Sponsor
Maastricht University Medical Center
Who can join
Adults 40 to 60, any sex, with Cognitive Impairment or Overweight and Obesity. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to investigate the effects of daily supplementation of Brainport for a period of 6 months on cognitive health.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
The Effect of Long-Term <i>Aronia</i> <i>melanocarpa</i> Extract Supplementation on Cognitive Performance, Mood, and Vascular Function: A Randomized Controlled Trial in Healthy, Middle-Aged Individuals.
Ahles S, Stevens YR, Joris PJ, Vauzour D, et al · · 2020 · cited 30× · PMID 32824483 · DOI 10.3390/nu12082475
Verify or expand the search:
- PubMed search for NCT03236259
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Maastricht University Medical Center trials
Trials by the same sponsor.
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- NCT04597892 — Efficacy of Point-Of-Care Creatinine Assays in Patients With eGFR <30 Receiving Intravascular Contrast · withdrawn
- NCT07287358 — Optimal Cerebral Perfusion Pressure Guided Therapy: Assessment of Target Effectiveness - II · NA · not yet recruiting
- NCT07501780 — Real-world Evaluation of the Implementation of LC-OCT in Daily Clinical Practice · not yet recruiting
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 NCT03236259 (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 Maastricht University Medical Center
- Last refreshed: 25 February 2021
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/NCT03236259.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing