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COMPLETED Phase 2

Postmenopausal Women and Their Endothelium

NCT03644472 · View on ClinicalTrials.gov ↗

Study Summary

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.

Conditions Studied

Interventions

  • DRUG nitrate rich beetroot juice
  • DRUG nitrate depleted beetroot juice

Study Locations (1)

Pennsylvania

  • Penn State University — University Park

Trial Details

FieldValue
Enrollment Target 37 participants
Start Date 2018-11-07
Est. Completion 2023-02-20
Phase Phase 2

Sponsor

Penn State University

233 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03644472

The ClinicalTrials.gov registry entry for NCT03644472 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 37 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Penn State University, which has 233 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Postmenopausal Women appearing as the primary indexed condition, and to 2 interventions — of which nitrate rich beetroot juice is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03644472 reports 1 study location spanning 1 distinct geographic area — top geographies include Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03644472 about?

NCT03644472 is a clinical study titled "Postmenopausal Women and Their Endothelium". 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 vi...

What is the current status of trial NCT03644472?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 37 participants. The study started on 2018-11-07. Estimated completion is 2023-02-20.

What conditions does trial NCT03644472 study?

This clinical trial studies the following conditions: Postmenopausal Women. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03644472?

The interventions under investigation include: nitrate rich beetroot juice (DRUG), nitrate depleted beetroot juice (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03644472?

This trial is sponsored by Penn State University, which has 233 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03644472 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial