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COMPLETED NA

A Study of High-Dose Vit D Versus Standard of Care Vit D Supplementation

NCT05016310 · View on ClinicalTrials.gov ↗

Study Summary

This is a randomized study evaluating the effects of early intensive vitamin D supplementation compared to standard of care vitamin D supplementation on bone health over an 18 month period.

Interventions

  • DIETARY_SUPPLEMENT High Dose Vitamin D
  • DIETARY_SUPPLEMENT Standard of Care Vitamin D

Study Locations (1)

North Carolina

  • Levine Cancer Institute — Charlotte

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2021-09-16
Est. Completion 2024-08-15
Phase NA

Sponsor

Wake Forest University Health Sciences

1,061 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05016310

The ClinicalTrials.gov registry entry for NCT05016310 describes a study currently listed as completed. 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 7 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,061 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Breast Cancer appearing as the primary indexed condition, and to 2 interventions — of which High Dose Vitamin D 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: NCT05016310 reports 1 study location spanning 1 distinct geographic area — top geographies include North Carolina. 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 NCT05016310 about?

NCT05016310 is a clinical study titled "A Study of High-Dose Vit D Versus Standard of Care Vit D Supplementation". This is a randomized study evaluating the effects of early intensive vitamin D supplementation compared to standard of care vitamin D supplementation on bone health over an 18 month period.

What is the current status of trial NCT05016310?

This trial is currently completed. It is a NA study. The enrollment target is 7 participants. The study started on 2021-09-16. Estimated completion is 2024-08-15.

What conditions does trial NCT05016310 study?

This clinical trial studies the following conditions: Breast Cancer, Osteoporosis, Breast. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05016310?

The interventions under investigation include: High Dose Vitamin D (DIETARY_SUPPLEMENT), Standard of Care Vitamin D (DIETARY_SUPPLEMENT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05016310?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,061 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05016310 being conducted?

This trial has 1 study location across North Carolina. 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