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Percent agreement of vital signs monitoring between the experimental sensor and standard of care monitoring
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| wearable vital signs sensor | Device | vital signs monitoring during maternal non-stress testing |
| Measure | Description | Time Frame |
|---|---|---|
| Device comparison to standard monitoring | The primary outcome measure is concordance of FHR tracing assessments from Rogers sensor recordings with those obtained from the current standard of care electronic fetal monitoring systems. | 3 years |
| Measure | Description | Time Frame |
|---|---|---|
| Qualitative analyses of sensor output | Qualitative analyses of FHR, MHR, BP, pulse oximetry, and UC data capture from the sensors will be performed for the purpose of optimizing signal-to-noise filtering of raw data collected during the study. Any adverse events will be recorded such as skin irritation (expected to be negligible). | 3 years |
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Inclusion Criteria:
Exclusion Criteria:
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Pregnant women
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Northwestern Medicine Prentice Women's Hospital | Chicago | Illinois | 60611 | United States |
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