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Alternative Treatments of Vitamin D Deficiency

Not Applicable
Completed
Conditions
Vitamin D Deficiency
Registration Number
NCT01512537
Lead Sponsor
Lund University
Brief Summary

The purpose of the study is to compare the efficiency of UVB and vitamin D supplementation in treatment of vitamin D deficiency.

Detailed Description

Patients with vitamin D deficiency were recruited and randomized into two groups, one exposed to UVB and the other receiving oral treatment with vitamin D supplementation.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
32
Inclusion Criteria
  • Vitamin D deficiency (< 25 nmol/l)
  • Age 15 or above
Exclusion Criteria
  • Travel south of 45 degrees latitude during the trial.
  • Ongoing treatment with vitamin D supplementation.
  • Intake of light sensitive medicine, such as tetracyclins.
  • Skin light eruptions

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Vitamin D (nmol/l).Week 0

Vitamin D was measured in a bloodsample to determine baseline status.

Vitamin D (nmol/l)Week 3

Vitamin D was measured in a bloodsample to follow the change from baseline in vitamin D level at week 3.

Vitamin DWeek 6

Vitamin D was measured in a bloodsample to follow the change from baseline in vitamin D level at week 6.

Secondary Outcome Measures
NameTimeMethod
Parathyroid hormone (pmol/l).Week 0, 3 and 6.

To investigate whether parathyrodiea hormone changes during the study.

Albumin (g/l).Week 0, 3 and 6.

To investigate whether albumin changes during the study.

Calcium (mmol/l)Week 0, 3 and 6.

To investigate whether calcium changes during the study.

Hemoglobin A 1c (percentage HbA1c of total hemoglobin).Week 0, 3 and 6.

To investigate whether HbA1c changes during the study.

Trial Locations

Locations (1)

Department of Dermatology, Lund University Malmoe

🇸🇪

Malmoe, Sweden

Department of Dermatology, Lund University Malmoe
🇸🇪Malmoe, Sweden

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