Neurosonographic Findings in Pregnant Women With Vitamin D Deficiency
Evaluation of Neurosonographic Findings in Pregnant Women With Vitamin D Deficiency
1 other identifier
observational
100
1 country
1
Brief Summary
In the study, the potential effects of vitamin D deficiency on fetal neurodevelopmental parameters will be examined. In this context, fetal brain development will be compared between pregnant women with and without vitamin D deficiency, revealing the possible neurodevelopmental outcomes of vitamin D deficiency during the prenatal period.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Mar 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 15, 2025
CompletedFirst Submitted
Initial submission to the registry
March 24, 2025
CompletedFirst Posted
Study publicly available on registry
March 30, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
November 30, 2025
CompletedNovember 18, 2025
November 1, 2025
4 months
March 24, 2025
November 16, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pregnant women with vitamin D deficiency who present for routine antenatal care between 20-30 weeks of gestation.
Neurosonogram Results Performed Between 20-30 Weeks of Gestation.
Study Arms (1)
Pregnant women with vitamin D deficiency who present for routine antenatal care between 20-30 weeks
Interventions
Comparison of Neurosonographic Findings in Patients with and without Vitamin D Deficiency.
Eligibility Criteria
Patients presenting to the Perinatology clinic of Şanlıurfa Training and Research Hospital for routine antenatal care between 20-30 weeks of gestation will be included.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sanliurfa Education and Research Hospital
Sanliurfa, 63100, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Target Duration
- 4 Months
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 24, 2025
First Posted
March 30, 2025
Study Start
March 15, 2025
Primary Completion
June 30, 2025
Study Completion
November 30, 2025
Last Updated
November 18, 2025
Record last verified: 2025-11
Data Sharing
- IPD Sharing
- Will not share