VIDIS: 25- Hydroxyvitamin D Levels in Pregnancy and Effects on Pregnancy Related Disorders
Sponsor
Medical University of Vienna (Other)
Overall Status
Completed
CT.gov ID
NCT04637880
Collaborator
Ratiopharm GmbH (Industry)
249
1
72
3.5
Study Details
Study Description
Brief 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
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
249 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
25- Hydroxyvitamin D Levels in Pregnancy and Effects on Pregnancy Related Disorders
Study Start Date
:
Jul 1, 2012
Actual Primary Completion Date
:
Jul 1, 2018
Actual Study Completion Date
:
Jul 1, 2018
Outcome Measures
Primary Outcome Measures
- 25- Hydroxyvitamin D and relation to development of preeclampsia [over course of pregnancy]
Secondary Outcome Measures
- 25 Hydroxyvitamin D in newborn [once at delivery]
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
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
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Department of Obstetrics and fetomaternal Medicine, Medical University of Vienna | Vienna | Austria | 1090 |
Sponsors and Collaborators
- Medical University of Vienna
- Ratiopharm GmbH
Investigators
- Principal Investigator: Harald Zeisler, Univ. Prof. Dr., MUV
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Julia Wild, MD,
Dr. med. univ,
Medical University of Vienna
ClinicalTrials.gov Identifier:
NCT04637880
Other Study ID Numbers:
- V02
First Posted:
Nov 20, 2020
Last Update Posted:
Nov 20, 2020
Last Verified:
Nov 1, 2020
Additional relevant MeSH terms: