Research for development of non-invasive fetal pulse oximetry
- Conditions
- not applicable
- Registration Number
- DRKS00024652
- Lead Sponsor
- Zentralklinikum Suhl GmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 10
Inclusion Criteria
1. subject = 18 years
2. pregnancy from the 24th gestation week
3. subject with intact skin in the abdominal region
4. voluntary participation and written informed consent form
Exclusion Criteria
1. subject < 18 years
2. pregnancy before the 24th gestation week
3. multiple pregnancy
4. skin infection or open wounds in the abdominal region
5. blood pressure = 160/110 mm Hg
6. subject with active implantats (e.g. cardiac stimulator, cochlea implantat, neurostimulator, insulin pump)
7. known or supposed alcohol and nicotine abuse
8. acute obstetric complications (e.g. intense vaginal bleedings, labour, rupture of the membranes)
9. study participation = 28 days before start of measurements
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method development of algorithms for signal separation of maternal and fetal pulses
- Secondary Outcome Measures
Name Time Method development of algorithms for the detemination of the fetal oxygen saturation