To study central blood pressure changes caused by commonly used high blood pressure
medications in pregnancy.
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Locations near you
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Full eligibility criteria for NCT02912910
Ages eligible for Study
14 Years to 50 Years
Genders eligible for Study
Accepts Healthy Volunteers
Women with hypertensive disease in pregnancy who are currently being treated with nifedipine xl or labetalol
Currently on multiple anti-hypertension medications
Irregular heart rhythms or arrhythmias
Peripheral arterial disease, leg artery disease
If there is a wound at location of where central arterial cuff would be placed or tonometer for carotid assessment
Known sensitivity to labetalol or nifedipine
Severe tachycardia (>120)
Greater than 1st degree heart block
Congestive heart failure or heart disease
Inability to adequately monitor BP
Currently receiving magnesium sulfate
All locations for NCT02912910
View full eligibility
Tris trial is registered with FDA with number: NCT02912910. The sponsor of the trial is St. Louis University and it is looking for 0 volunteers for the current phase.
Official trial title: Changes in Central Arterial Pressure When Comparing Nifedipine and Labetalol for Routine Hypertension Control in Pregnancy
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