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NCT04637880 Clinical Trial

25- Hydroxyvitamin D Levels in Pregnancy and Effects on Pregnancy Related Disorders

Vitamin d Deficiency Clinical Trial

— VIDIS  

Official title:
25- Hydroxyvitamin D Levels in Pregnancy and Effects on Pregnancy Related Disorders

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04637880
Other study ID # V02
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 2012
Est. completion date July 1, 2018

Study information
Verified date November 2020
Source Medical University of Vienna
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Evaluation of 25- Hydroxyvitamin D levels in pregnant women in Austria and potential related disorders Hypothesis: Austrian pregnant women are Vitamin D deficient Present vitamin D supplementation in pregnancy is insufficient Vitamin D deficiency is associated with pregnancy related disorders like preeclampsia

Recruitment information / eligibility
Status Completed
Enrollment 249
Est. completion date July 1, 2018
Est. primary completion date July 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - age> 18 years - informed consent Exclusion Criteria: - chronic hypertension - kidney disease - lupus erythematodes - diabetes mellitus - malabsorption syndrome - hyperparathyroidism - surgery on the thyroid gland

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Austria Department of Obstetrics and fetomaternal Medicine, Medical University of Vienna Vienna

Sponsors (2)
Lead Sponsor Collaborator
Medical University of Vienna Ratiopharm GmbH

Country where clinical trial is conducted

Austria, 

Outcome
Type Measure Description Time frame Safety issue
Primary 25- Hydroxyvitamin D and relation to development of preeclampsia over course of pregnancy
Secondary 25 Hydroxyvitamin D in newborn once at delivery
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