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OpenTrials
Completed

NCT Number: NCT02677233

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

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

Completed

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. vitamin D level in preeclamptic and non preeclamptic women

    Time frame: six months

Sponsors and collaborators

Lead sponsor

Ain Shams Maternity Hospital

Other

Registry information

Important dates

Study start
2015
Primary completion
2015
Study completion
2016
First posted
Feb 9, 2016
Registry last updated
Feb 9, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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