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Solius UV Light Source in Improving Serum Levels of 25-hydroxyvitamin D

NCT04865432 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2022-12-23

Study results available
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Summary

This is a feasibility interventional study seeking to determine the safety and efficacy of the Solius Photobiologic System in increasing the serum levels of 25(OH)D in a vitamin D deficient/insufficient adult population.

Conditions

  • Vitamin D Deficiency
  • Vitamin D Insufficiency

Interventions

DEVICE

UVB treatment

5 weeks of UVB titration to determine individual's UVB sensitivity followed by 4 weeks of UVB exposure intervention

Sponsors & Collaborators

  • Boston University

    lead OTHER

Principal Investigators

  • Michael Holick, PhD MD · Boston University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-08-24
Primary Completion
2021-12-12
Completion
2021-12-12
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04865432 on ClinicalTrials.gov