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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04013399
Other study ID # 201905166
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date July 1, 2020
Est. completion date March 30, 2023

Study information

Verified date July 2023
Source Barnes-Jewish Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will evaluate the effect of treatment of obstructive sleep apnea on insulin sensitivity in pregnant women. Women in their third trimester of pregnancy will be randomized to receive treatment or no treatment for one month.


Description:

Obstructive Sleep Apnea (OSA) worsens over pregnancy and is related to increased risk of gestational diabetes. Despite the fact that sleep disturbances are common during pregnancy, OSA remains under-diagnosed, and poorly understood particularly in pregnancies affected by obesity. At least 25 percent of pregnancies are now affected by obesity, a leading risk factor for OSA, yet the effect of treatment of OSA on patterns of metabolic function and specifically decreased insulin sensitivity in pregnant women with obesity is a neglected area with major therapeutic implications to improve maternal health. Inflammation with OSA may decrease insulin sensitivity. Continuous positive airway pressure (CPAP) is a known effective treatment for OSA and has been shown to improve insulin sensitivity outside of pregnancy. Our overall hypothesis is that, compared with standard care, CPAP will improve nighttime breathing, blood and tissue oxygenation, decrease markers of inflammation, and increase insulin sensitivity. Using a randomized controlled trial, we will determine the effect of CPAP on metabolic dysfunction induced by OSA in pregnant women with obesity.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date March 30, 2023
Est. primary completion date September 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 39 Years
Eligibility Inclusion Criteria: - 28-32 weeks pregnant - Age 20-39 - BMI 30-40 kg/m2 pre-pregnancy (or first trimester) - Obstructive Sleep Apnea (AHI=15) - Have a singleton pregnancy Exclusion Criteria: - Diabetes (GDM, type 1 or type 2) - Using beta blockers or glucocorticoids - Have children who are =2 yrs old (risk of disrupted sleep) - Diagnosed sleep disorders (other than sleep apnea) - Night work schedule - Diagnosed congestive heart failure - Diagnosed lung disease (e.g. asthma, chronic obstructive pulmonary disease) - Pre-gestational hypertension

Study Design


Intervention

Device:
Continuous Positive Airway Pressure
The device is an auto-adjusting pressure device with an integrated humidifier. Pressure is adjusted based on airway resistance.

Locations

Country Name City State
United States Washington University in St. Louis Saint Louis Missouri

Sponsors (2)

Lead Sponsor Collaborator
Barnes-Jewish Hospital Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Degree of Insulin Sensitivity measured by Matsuda Index by Oral glucose Tolerance Test Change in whole body insulin sensitivity measured using Matsuda Index 1 month
Primary Percent of Oxygen in blood by pulse oximetry Change in oxygen saturation measured by pulse oximetry 1 month
Secondary Percent of Oxygen in Adipose Tissue measured by oxygen tension probe Change in adipose tissue oxygenation measured by oxygen tension 1 month
Secondary Concentration of inflammatory gene expression in adipose Tissue measured by RNA and DNA sequencing Change in adipose tissue gene expression of inflammatory markers 1 month
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