Association Between Vitamin D Deficiency and Preeclampsia: A Case Control Study

Pre-Eclampsia Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02677233
• Other study ID #: vid-20
• Status: Completed
• Phase: N/A
• First received: February 5, 2016
• Last updated: February 5, 2016
• Start date: June 2015
• Est. completion date: January 2016

Study information

• Verified date: February 2016
• Source: Ain Shams Maternity Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: Egypt: Ministry of Higher Education
• Study type: Observational

Clinical Trial Summary

To find out if lower levels of vitamin D is more prevalent in preeclamptic women

Recruitment information / eligibility

• Status: Completed
• Enrollment: 90
• Est. completion date: January 2016
• Est. primary completion date: December 2015
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 35 Years

Eligibility

Inclusion Criteria:

• Parity: primigravida.

• Age: 18 - 35 years.

• Singleton pregnancy.

• Gestational age: 36-40 weeks.

• No past history of any medical disorder and with no other medical complications during pregnancy

Exclusion Criteria:

• Women with preexisting medical conditions like rheumatoid arthritis, thyroid, hepatic or renal failure, metabolic bone disease, diabetes mellitus, malabsorption and lupus.

• History of intake of medications influencing bone, vitamin D or calcium metabolism e.g. antiepileptic, theophylline, antitubercular drugs in the last 6 months.

• Women with multiple pregnancy.

• Women with congenital fetal malformation.

• Women with known thrombophilia

Study Design

Observational Model: Case Control, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Pre-Eclampsia

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Ain Shams Maternity Hospital

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	vitamin D level in preeclamptic and non preeclamptic women		six months	No