Overview

Impact of Antichlamydial Treatment on the Rate of Preeclampsia

Status:
Unknown status
Trial end date:
2018-08-01
Target enrollment:
0
Participant gender:
Female
Summary
This randomized, double blinded controlled trial included 1200 healthy primigravidae who attended an outpatient clinic at 16-20weeks of pregnancy. All women were randomly divided equally into two groups, group A(600 women) who received antichlamydial treatment in the form of azithromycin 1 gram single oral dose before 20 weeks of pregnancy and group B (600 women) who received no treatment(placebo). All participants were followed up for up to 6 weeks postpartum and observed for the development of preeclampsia.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Ain Shams Maternity Hospital
Treatments:
Azithromycin
Criteria
Inclusion Criteria:

- primigravida, singleton pregnancy, maternal age 18-35 years, and pregnancy duration
16-20 weeks at the time of study inclusion.

Exclusion Criteria:

- Women with multi-fetal pregnancy, diabetes mellitus, chronic hypertension, or chronic
renal disease