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A Comparison of Capsules and Oral Spray Solution as Methods of Delivering Vitamin D3 and Raising Status (SCD3)

U

Ulster University

Status

Completed

Conditions

Vitamin D Status
Vitamin D Concentration

Treatments

Dietary Supplement: 3000IU(75μg) vitamin D3

Study type

Interventional

Funder types

Other

Identifiers

NCT02608164
REC/15/0083

Details and patient eligibility

About

The aim of the study is to compare the effectiveness of a vitamin D3 oral spray solution with capsules at raising vitamin D status over winter.

This randomised crossover trial will aim to recruit a total of 22 healthy participants for a total of two 4-week interventions separated by a 10-week washout.

Enrollment

22 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Apparently healthy
  • Over the age of 18

Exclusion criteria

  • Those that intend to consume a supplement containing vitamin D at any point during the study
  • Those under the age of 18.
  • Individuals that are on prescribed medication that is known to affect vitamin D metabolism
  • Those following a vegan diet
  • Sun-bed users
  • Participants that are planning a sun holiday during the study

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

22 participants in 2 patient groups

Vitamin D oral spray solution
Active Comparator group
Description:
An oral spray solution containing 3000IU (75micrograms) vitamin D3 per spray
Treatment:
Dietary Supplement: 3000IU(75μg) vitamin D3
Vitamin D capsules
Active Comparator group
Description:
A capsule containing 3000IU (75micrograms) vitamin D3 per capsule
Treatment:
Dietary Supplement: 3000IU(75μg) vitamin D3

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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