Clinical trial

Predictors of De-novo Development of Obstructive Sleep Apnea in Pregnancy

Active, not recruiting · Not applicable · 1 countries · Registry ID NCT02917876

Active, not recruitingNot applicableObservational

What this study is about

This study seeks to understand the physical, physiologic and biologic features that predispose a woman to the development of obstructive sleep apnea once they are exposed to the cardiopulmonary and metabolic physiological changes of pregnancy. Knowing these specific predictive factors can help identify a population at risk and guide clinicians to develop suitable targeting screening strategies.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to Not listed

SexFemale

Healthy volunteersNot accepted

ConditionObstructive Sleep Apnea, Pregnancy, Obesity, Sleep

Full registry criteria

Inclusion Criteria: * \<13 completed weeks of gestation * BMI \>30 kg/m2 at recruitment * \>18 years of age * Ability to give informed consent Exclusion Criteria: * Unable to meet inclusion criteria * Twin pregnancies

Treatments and study arms

The registry does not list a named intervention.

Primary outcomes

Characteristics of participants who develop obstructive sleep apnea defined as an apnea hypopnea index >5 events per hourUp to 40 weeks

The study will develop a model of biologic, physiologic and anthropometric measures that predict the development of obstructive sleep apnea apnea later in pregnancy compared to baseline in early pregnancy.

Study locations

1 locations were listed when this page was built. The first 40 are shown.

The Miriam Hospital🇺🇸 Providence, Rhode Island, United States

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