Dexamethasone and Pregnancy: Maternal Effects

Recruiting Observational Study
Dexamethasone During Pregnancy
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Female
Study type
Observational
Participants needed
35 (estimated)
Sponsor
Assistance Publique - Hôpitaux de Paris · Other
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About This Trial
This study will analyze obstetric, endocrine and metabolic follow-up data in women treated with DEX. It will reveal the prevalence and importance of weight gain, insomnia, edema, stretch marks, arterial hypertension and gestational diabetes, describe pregnancy outcome, and analyze the corticotropic axis during and up to 3 months after pregnancy, with the aim of improving the management of these wo…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Femme majeure (âge ≥ 18 ans) 2. Grossesse avec indication de traitement anténatal par dexaméthasone (DEX) en accord avec le PNDS : * Mutation sévère du gène CYP21A2 chez chacun des parents * Fœtus féminin 3. Grossesse unique 4. Ayant commencé un traitement anténatal pa…
Contacts

Anne BACHELOT, Pr

01 42 16 02 46

anne.bachelot@aphp.fr

CONTACT

Imene HADDADOU, CP

01.42.16.24.98

imene.haddadou@aphp.fr

CONTACT