Utilization of Somatic Tissue Oxygen Saturation Monitoring in Pregnant Women
Withdrawn before enrolling · Not applicable
Conditions studied: Pre-Eclampsia
In brief
The purpose of this study is to compare 3 methods of assessing endothelial function in healthy female volunteers and pregnant women with and without pregnancy induced hypertension. The methods under comparison are simultaneous tissue oxygen saturation (StO2), EndoPAT and Sphygmocor (pregnant women only). 35 participants (15 healthy, 10 pregnant normal blood pressure, 10 pregnant with hypertension) will be enrolled.
Key facts
- Study ID
- NCT03196141
- Run by
- Yale University
- People needed
- 0
- Starts
- 2018-10-01
- Expected to finish
- 2019-10-01
- Last updated by the study team
- 2019-07-12
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Non-pregnant group:
- > 18 years of age
- Male or female
- Pregnant group:
- > 18 years of age
- Pregnant women > 20 weeks
- Diagnosis of Pre-eclampsia characterized as Systolic BP > 140 mmHg, diastolic BP > 90 mmHg after 20 weeks of gestation accompanied by new onset of proteinuria.
- Normotensive, not meeting criteria in #3
You may not qualify if…
- Non-pregnant group:
- Raynaud's Disease
- Adhesive tape allergy
- Recent Myocardial Infarction (< 3 months)
- Congestive Heart Failure
- Pregnant group:
- Raynaud's Disease
- Adhesive tape allergy
- Recent Myocardial Infarction (< 3 months)
- Congestive Heart Failure
- Hemodynamically unstable (SBP < 90 mmHg)
- Fetal distress
Where it is running
- Yale-New Haven Hospital — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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