Acute Control of Chronic Hypertension



Status:Recruiting
Conditions:High Blood Pressure (Hypertension), Women's Studies
Therapuetic Areas:Cardiology / Vascular Diseases, Reproductive
Healthy:No
Age Range:18 - Any
Updated:3/20/2019
Start Date:February 18, 2019
End Date:July 1, 2021
Contact:Johanna Bringley, DO
Email:bringlj@amc.edu
Phone:518.262.4942

Use our guide to learn which trials are right for you!

Acute Control of Chronic Hypertension in Preeclampsia

The purpose of this study is to understand if administration of a personalized dose of the
anti-hypertensive medication, labetalol, based on patient's history of preexisting
hypertension, will be more effective at controlling severe hypertension during pregnancy,
compared to the current standard dosing.

The investigators seek to asses the effect of preexisting hypertension on the patient's
response to treatment for severe hypertension in preeclampsia with severe features. The
investigators hypothesize that successive administration of 40-60-80 mg of labetolol will
reduce time to blood pressure control versus the standard dosing, 20-40-80 mg labetolol,
recommended by the American College of Obstetricians and Gynecologists in 2015.

Inclusion Criteria:

- Age ≥ 18 years

- Gestational age ≥ 24 weeks

- Singleton gestation

- Chronic hypertension as defined as two elevated blood pressures (SBP ≥ 140mmHg and/or
DBP ≥ 90mmHg) at least 4 hours apart before 20 weeks gestation

Exclusion Criteria:

- Known allergic reaction to labetalol

- Persistent mild-moderate asthma (≥ 2 rescue inhaler uses per week in the previous
month)

- Obstructive airway disease

- Bradycardia < 70 beats/min

- Heart block > 1st degree or history of heart failure
We found this trial at
1
site
Albany, New York 12208
Phone: 518-262-4942
?
mi
from
Albany, NY
Click here to add this to my saved trials