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NCT06413576Completed

Homocysteine in Critically Ill Preeclampsia

The Clinical Utility of Homocysteine in Critically Ill Preeclampsia Patients

Source: ClinicalTrials.gov · Last updated 7 Apr 2026

Brief summary (registry, in English)

Preeclampsia is a disorder characterized by the new onset of hypertension and proteinuria typically presenting after 20 weeks of gestation. Elevated circulating homocysteine is a risk factor for endothelial dysfunction and vascular diseases such as atherosclerosis and occlusive disorders. Our study is to investigate the association between elevated blood homocysteine levels and complications in pregnant women in order to conclude the clinical utility of homocysteine as a marker of severity in the cases of pre-eclampsia.

Status (registry)
Completed
Study type
Observational
Enrollment
70 (actual)
First submitted
6 Apr 2024
Start date
19 Jan 2024
Primary completion date
10 Apr 2025
Lead sponsor
Ain Shams University
NCT number
NCT06413576

What you commit to

  • Study type: Observational
  • Participants enrolled: 70
  • From 19 Jan 2024 to the primary completion date, 10 Apr 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • On treatment with antifolate drugs such as methotrexate

Other illness

  • Essential hypertension suggested by history or documentation of hypertension in pre pregnant state or hypertension before 20 weeks of gestation.
  • Cardiovascular or renal failure
  • Liver failure
  • Diabetes mellitus
  • Inflammatory or infective disorders
  • History or documentation of epilepsy in prepregnant state

Other

  • Space occupying lesion in brain like tuberculoma or brain tumor
  • Trauma to brain
  • Hyperpyrexia

Who the study is looking for

  • All patients diagnosed by preeclampsia will be included in light of the following diagnostic criteria (blood pressure more than 140\\90 mm\\Hg on 2 occasions at least 4 hours apart after 20 weeks' gestation in a previously normotensive patient accompanied by Protein/creatinine ratio ≥0.3 .

Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ain Shams University
Coordinator of this site? Confirm its status
CairoEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.