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Oral Vitamin D Supplementation in Elderly Women

U

University of Helsinki

Status

Completed

Conditions

Optimal Vitamin D Administration

Treatments

Dietary Supplement: vitamin D twice daily
Dietary Supplement: Vitamin D3 oil three times in a year

Study type

Interventional

Funder types

Other

Identifiers

NCT00575835
77/2006

Details and patient eligibility

About

The aim of this study is to compare oral vitamin D supplementation administered in two different ways, namely either twice a day (800IU/d, 292000IU/y) or three times a year (97333IU every 4 months, 292000IU/y) in elderly women in combination with daily supplementation of calcium 1 gram. We will 1)compare the blood concentrations of 25 OH vitamin D in the two treatment groups amd monitor if a sufficient and safe concentration of 25OH D in blood can be maintained with these two treatments.2) Find out seasonal variation in vitamin D concentrations in these treatments. 3) Find out safety of these treatments

Enrollment

40 patients

Sex

Female

Ages

70 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Females
  • 70-80 years
  • Living in the community

Exclusion criteria

  • Renal disease
  • Diseases that contraindicate vitamin D supplementation
  • Medications affecting bone
  • Malignancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 2 patient groups

1
Active Comparator group
Treatment:
Dietary Supplement: vitamin D twice daily
2
Experimental group
Treatment:
Dietary Supplement: Vitamin D3 oil three times in a year

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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