Mechanisms of Increased Ambulatory Blood Pressure in Patients With Intradialytic Hypertension (NCT01862497) | Clinical Trial Compass
CompletedNot Applicable
Mechanisms of Increased Ambulatory Blood Pressure in Patients With Intradialytic Hypertension
United States76 participantsStarted 2013-01
Plain-language summary
The purpose of this study is 1) to determine what physiologic factors (extracellular fluid overload or vasoconstriction) contribute more to increased blood pressure levels between dialysis treatments in hemodialysis patients whose blood pressure increases and decreases during hemodialysis and 2) to determine whether carvedilol provides better control of blood pressure between dialysis treatments than prazosin in patients whose blood pressure increases during dialysis.
Who can participate
Age range18 Years – 80 Years
SexALL
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Inclusion Criteria (for Aims 1 and 2):
* age more than 18 years
* Hypertension defined as systolic blood pressure more than 140 mmHg before dialysis or more than 130 mmHg after dialysis
* For case subjects with intradialytic hypertension: systolic blood pressure increase more than 10 mmHg from pre to post dialysis in at least 4 out of 6 screening treatments
* For control subjects: systolic blood pressure decrease more than 10 mmHg from pre to post dialysis in at least 4 out of 6 screening treatments
Inclusion criteria for Aim 3 includes the case subjects described above.
Exclusion Criteria:
For Aims 1 and 2:
* Hemodialysis vintage less than 1 month
* Amputated arm or leg
* Presence of cardiac defibrillator or pacemaker
* Presence of large metal prosthesis
* Failure to achieve dry weight
For Case subjects participating in Aim 3:
* Patients with a specific indication for beta blocker therapy including systolic heart failure, history of myocardial infarction, history of tachyarrhythmia or angina being managed with beta blocker therapy.
* Patients with contraindications to beta blockade including bradycardia (heart rate less than 60 beats per minute) while not on a pulse lowering drug, severe reactive airway disease, prior intolerance to beta blocker therapy
* Prior intolerance to alpha blocker therapy
What they're measuring
1
Ratio of Extracellular Body Water to Total Body Water
Timeframe: Expected recruitment is 4-5 years
Trial details
NCT IDNCT01862497
SponsorUniversity of Texas Southwestern Medical Center