Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Elucidating the Minimal Effective Dose of Prunes for Bone Health in Postmenopausal Women

NCT06184646 · View on ClinicalTrials.gov ↗

Study Summary

The objective of this study is to examine if calcium and vitamin D supplements and/or prune can prevent bone loss in postmenopausal women.

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT Prune

Study Locations (1)

California

  • San Diego State University — San Diego

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2024-03-15
Est. Completion 2028-12
Phase NA

Sponsor

San Diego State University

201 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06184646

The ClinicalTrials.gov registry entry for NCT06184646 describes a study currently listed as recruiting. It is categorized as NA, 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 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is San Diego State University, which has 201 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 Bone Disease, Metabolic appearing as the primary indexed condition, and to 1 intervention — of which Prune 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: NCT06184646 reports 1 study location spanning 1 distinct geographic area — top geographies include California. 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 NCT06184646 about?

NCT06184646 is a clinical study titled "Elucidating the Minimal Effective Dose of Prunes for Bone Health in Postmenopausal Women". The objective of this study is to examine if calcium and vitamin D supplements and/or prune can prevent bone loss in postmenopausal women.

What is the current status of trial NCT06184646?

This trial is currently recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2024-03-15. Estimated completion is 2028-12.

What conditions does trial NCT06184646 study?

This clinical trial studies the following conditions: Bone Disease, Metabolic. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06184646?

The interventions under investigation include: Prune (DIETARY_SUPPLEMENT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06184646?

This trial is sponsored by San Diego State University, which has 201 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06184646 being conducted?

This trial has 1 study location across California. 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