Finding studies
Finding studies
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Luisa Rios-Avila
CONTACT
Ernest Ayers, MSPH
CONTACT
Lead
University of Washington
With
This is a randomized trial of patients who are receiving in-center hemodialysis treatments for end stage kidney disease and have clinical suspicion of fluid overload. Enrolled participants will be randomly assigned in 1:1:1 fashion to either a four-week ultrafiltration strategy, an eight-week ultrafiltration strategy, or continuation of their regular thrice weekly hemodialysis treatments. Each ultrafiltration strategy will add two extra four-hour ultrafiltration treatments per week plus pharmacist-guided tapering of blood pressure medications. We will test the impact of these strategies on primary outcomes of 1. Change in 24-hour continuous ambulatory blood pressure from baseline to 24-weeks 2. Change in symptoms of congestion from baseline to 24-weeks We will also test the impact of the treatment strategies on related symptoms, physical activity levels, hemodynamics. and measures of safety.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
