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Pregnancy, Sleep Disordered Breathing and Peripartum Complications

Is Sleep Disordered Breathing During Pregnancy a Modifiable Risk Factor for Fetal Growth Restriction?

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02651649
Enrollment
50
Registered
2016-01-11
Start date
2016-02-29
Completion date
2018-12-31
Last updated
2016-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy, Sleep Apnea

Brief summary

Sleep disordered breathing (SDB) during pregnancy is a modifiable risk factor for poor maternal and fetal outcomes. The investigators propose a prospective observational study to assess the utility of continuous positive airway pressure (CPAP) administration (intervention) during pregnancy to reduce maternal and fetal morbidity. Secondarily, we will also perform a cohort study to assess the incidence of antenatal sleep-disordered breathing as measured by ambulatory sleep monitoring applied in the hospital setting.

Detailed description

Hypothesis: CPAP application in SDB-diagnosed parturients will decrease fetal and maternal morbidity. Specific Aims: 1\. To screen women after their first trimester of pregnancy that are at risk for carrying babies with fetal growth restriction (FGR) for presence of SDB (FGR is commonly diagnosed at 20 weeks gestation by ultrasound as standard of care) and to follow their diagnosis and treatment with CPAP, as per standard of care, for the remainder of their pregnancy or order to follow fetal and maternal outcomes. a. Screen = parturients affirm presence of snoring. b. Screen positive parturients are further assessed with 1-2 nights of ambulatory sleep and respiration monitor to confirm SDB b. SDB positive parturients are offered treatment, as per standard of care, with CPAP. c. Screen positive parturients are reassessed with 1-2 nights of ambulatory sleep monitoring (whether or not CPAP is eventually applied) at two more intervals during pregnancy (during second and third trimesters), and then 6-8 weeks after delivery. This study is designed as a prospective observational cohort study in order establish the concurrence of the disease (SDB) as it occurs with the increased risk or exposure to the vulnerable state (pregnancy) and presence of diagnosed fetal growth restriction. In addition, parturients who test positive for SDB will be assessed by a pulmonologist and offered standard of care therapy with CPAP, as appropriate. CPAP use will then be followed and assessed as a mitigating intervention to blunt fetal growth restriction. This study is a pilot in that we hope to establish the incidence of co-morbidities in order to appropriately plan for an adequate sample size in future intervention studies. Given the large overall parturient population that will be available to the study team, we believe that in one calendar year we will observe sufficient patients to establish the relationship of SDB during the antenatal pregnancy and fetal growth restriction.

Interventions

DEVICEContinuous Positive Airway Pressure (CPAP)

FGR diagnosed parturients who are diagnosed with OSA will be prescribed CPAP as per standard of care.

Sponsors

University of Rochester
CollaboratorOTHER
Hadassah Medical Organization
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* i. Prepartum * 18 years of age and older, able to provide informed consent * Pregnant * Diagnosis of fetal growth restriction (by ultrasound)

Exclusion criteria

* • Patient refusal * Inability to provide informed consent * Known maternal severe cardiopulmonary disease * Known fetal anomalies

Design outcomes

Primary

MeasureTime frameDescription
Presence of Fetal Growth Restriction at Birth6 monthsexpressed as a percentile of predicted weight

Secondary

MeasureTime frameDescription
Change in estimated fetal weight based on crossing nomograms6 monthsestimated growth of fetus by gestational age will be plotted and compared to group who did not receive CPAP

Contacts

Primary ContactYehuda Ginosar, M.D.
yginosar@icloud.com
Backup ContactSuzanne Karan, M.D.
suzanne_karan@urmc.rochester.edu058-692-0334

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026