Clinical Trials Directory

Trials / Completed

CompletedNCT04755322

Hydroxychloroquine in Prevention of Preeclampsia

Hydroxychloroquine is an Immunomodulator for Improvement of Pregnancy Outcomes in Preeclampsia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Assiut University · Academic / Other
Sex
Female
Age
20 Years – 40 Years
Healthy volunteers
Not accepted

Summary

Pre-eclampsia complicates up to 8% of pregnancies and is a major contributor to maternal mortality and morbidity The only effective treatment is delivery, which leads to significant neonatal morbidity and mortality if carried out preterm, especially when the disease occurs early in pregnancy. Vascular endothelial dysfunction and immunological impairment are associated with preeclampsia. To date, there is no effective or optimal therapeutic approach for these conditions. Hydroxychloroquine has endothelial protective action via ant diabetic, lipid lowering, antioxidant effects or direct endothelial protection. Hydroxychloroquine is an antimalarial and immunomodulatory agent. In pregnancy, hydroxychloroquine is prescribed for inflammatory conditions associated with adverse perinatal outcomes such as systemic lupus erythematosus, antiphospholipid syndrome and placental inflammatory lesions such as chronic histiocytic intervillositis, hydroxychloroquine has therapeutic potential to improve placental function in pregnancies associated with heightened inflammation.

Conditions

Interventions

TypeNameDescription
DRUGHydroxychloroquineHydroxychloroquine 400 mg at start of pregnancy
DRUGFolic acid5 mg
DRUGLow-dose aspirin75 mg

Timeline

Start date
2021-03-01
Primary completion
2023-07-30
Completion
2023-07-30
First posted
2021-02-16
Last updated
2023-12-08

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04755322. Inclusion in this directory is not an endorsement.

Hydroxychloroquine in Prevention of Preeclampsia (NCT04755322) · Clinical Trials Directory