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NCT03644472
Postmenopausal Women and Their Endothelium
Phase 2 trial testing nitrate rich beetroot juice in Postmenopausal Women in 37 participants. Completed in 20 February 2023.
20 February 2023
Quick facts
| Lead sponsor | Penn State University |
|---|---|
| Phase | Phase 2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | double |
| Primary purpose | basic science |
| Enrollment | 37 |
| Start date | 7 November 2018 |
| Primary completion | 20 February 2023 |
| Estimated completion | 20 February 2023 |
| Sites | 1 location across United States |
Drugs / interventions tested
- nitrate rich beetroot juice — full drug profile →
- nitrate depleted beetroot juice — full drug profile →
Conditions studied
- Postmenopausal Women — all drugs for Postmenopausal Women →
Sponsor
Penn State University
Who can join
Under 70, female only, with Postmenopausal Women. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to test the effects of a one time dose and 7-days of inorganic nitrate (supplied in the form of beetroot juice) on blood vessel function and resting blood pressure in healthy, postmenopausal women. Participants will drink beetroot juice and a placebo juice on separate visits where blood pressure and blood vessel function will be measured.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
A single dose of dietary nitrate supplementation protects against endothelial ischemia-reperfusion injury in early postmenopausal women.
Somani YB, Soares RN, Gosalia J, Delgado JM, et al · · 2022 · cited 15× · PMID 35358395 · DOI 10.1139/apnm-2021-0693 -
Seven-day dietary nitrate supplementation clinically significantly improves basal macrovascular function in postmenopausal women: a randomized, placebo-controlled, double-blind, crossover clinical trial.
Delgado Spicuzza JM, Gosalia J, Zhong L, Bondonno C, et al · · 2024 · cited 10× · PMID 38915856 · DOI 10.3389/fnut.2024.1359671
Verify or expand the search:
- PubMed search for NCT03644472
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Postmenopausal Women
Currently open trials in the same condition.
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- NCT06789900 — Everolimus and/or Exercise to Prevent Bone Loss in Postmenopausal Women · Phase 2 · active not recruiting
- NCT06042673 — Impact of Pomegranate Seed Oil on Postprandial Cardiovascular Disease Risk Markers · NA · recruiting
- NCT03705845 — Tocotrienols for Obesity of Postmenopausal Women · Phase 1, PHASE2 · active not recruiting
Other Penn State University trials
Trials by the same sponsor.
- NCT07147387 — Lions Hearts: A Community Approach to Multigenerational Cardiovascular Disease Risk · NA · not yet recruiting
- NCT07266506 — Development of an Eating Behavior Risk Score · NA · not yet recruiting
- NCT07229781 — Mediterranean Diet and Blood Sugar Study · NA · not yet recruiting
- NCT07235358 — Cardiometabolic Effects of Pecan Snacking in Prediabetes · NA · not yet recruiting
- NCT06823518 — Thrive Initiative Parent-Education Programming Study · NA · 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 NCT03644472 (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 Penn State University
- Last refreshed: 27 February 2023
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/NCT03644472.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing