Blood Pressure Clinical Trial
— BOLDOfficial title:
BOLD: A Trial of Blood Pressure Lowering in Dialysis
Verified date | June 2023 |
Source | University of California, San Francisco |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Blood pressure may be one of the most important modifiable risk factors for cardiovascular disease in patients with end-stage-renal-disease undergoing maintenance hemodialysis. Although a systolic blood pressure <140 mmHg treatment target has been recommended, there remains uncertainty on which blood pressure should be targeted, more specifically that measured in the dialysis unit or at home. Observational studies have reported a paradoxical U-shaped associated with dialysis unit (pre-dialysis) systolic blood pressure and cardiovascular events and death (where blood pressure below 140 mmHg is actually linked with poor outcomes). Conversely, the same studies have reported a linear association between higher home systolic blood pressure and worse clinical outcomes, where blood pressure below 140 mmHg is associated with better outcomes. This pilot clinical trial aims to address this important question.
Status | Completed |
Enrollment | 50 |
Est. completion date | December 6, 2018 |
Est. primary completion date | December 6, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 100 Years |
Eligibility | Inclusion Criteria: 1. Provision of signed and dated informed consent form 2. Undergoing in-center, thrice weekly hemodialysis for treatment of end-stage-renal-disease 3. Greater than 3 months since initiation of dialysis 4. Age 18 years or above 5. Able to obtain a brachial blood pressure at dialysis and at home Exclusion Criteria: 1. Pregnancy, anticipated pregnancy, or breastfeeding as this will require increase to more than three time a week dialysis and/or preclude use of some classes of blood pressure medications 2. Incarceration or institutionalized living which may prohibit measurement of home blood pressure 3. Participation in another intervention study that may affect blood pressure 4. Patients in whom systolic blood pressure is not measurable (e.g. those with left ventricular assist devices) 5. Hypotension: average pre-dialysis systolic blood pressure <100 mmHg over last 2 weeks prior to screening while not taking any blood pressure medications 6. Life expectancy <4 months 7. Anticipated living donor kidney transplant within 4 months |
Country | Name | City | State |
---|---|---|---|
United States | UCSF | San Francisco | California |
United States | University of Washington | Seattle | Washington |
Lead Sponsor | Collaborator |
---|---|
University of California, San Francisco | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), University of Washington |
United States,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Feasibility - Screen:Enrollment Ratio | Percentage of eligible participants screened and eventually enrolled in the study | Screening | |
Primary | Adherence to Assigned Treatment Arm | Percentage of participants in the home blood pressure (BP) arm who are able to measure home BP and transmit readings to the research team. Overall, across 16 wks. | 4 months | |
Primary | Number of Participants With Treatment-Emergent Adverse Events [Safety and Tolerability] | Postdialysis unit systolic BP <90 mmHg
Postdialysis unit systolic BP >200 mmHg Cramping during dialysis Syncope episodes Episodes of fall Episodes of flash pulmonary edema Symptoms of dizziness |
Assessed every 2 weeks over 4 months | |
Primary | Mean Duration (in Minutes) of Recovery From Dialysis Treatments | Data were reported at study visits every 2 wks, the mean was calculated from the first to the last follow-up visit. The mean was calculated for each participant, then the overall mean was calculated for each arm. | Assessed every 2 weeks; Data averaged over 16 weeks |
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