Could a better blood pressure reading save kidneys?
NCT ID NCT05163158
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study tested whether using central blood pressure (measured near the heart) instead of the usual arm cuff leads to better outcomes in 116 people with advanced chronic kidney disease. Participants were randomly assigned to either a central BP target or a standard arm BP target, both aiming for under 130 mmHg. The goal was to see if this approach is feasible and reduces artery stiffness after 12 months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Central blood pressure measurement
- What this could lead to
- If successful, this could show that using central blood pressure readings leads to better blood pressure management and fewer heart and kidney complications in advanced kidney disease patients.
- What could go wrong
- This is a small pilot study focused on feasibility, not on proving clinical benefits. The results may not confirm that central BP targeting is better than standard care, and larger trials are needed.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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116 people
The number who actually took part.
- Started
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May 2022
- Finished
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Jul 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Over 18 years of age; 2. eGFR \<30 mL/min/1.73m2 as determined by the CKD-EPI equation (within 30 days of screening); 3. Office brachial cuff systolic blood pressure between 120 and 160 mmHg (using automated office blood pressure). Exclusion Criteria: 1. Already taking 5 or more anti-hypertensive medications (any class) 2. Unwillingness to change anti-hypertensive medication by the attending Nephrologist or patient 3. Recent acute kidney injury (\>50% increase in serum creatinine in preceding 30 days) 4. Previous kidney replacement therapy (kidney transplant, hemodialysis or peritoneal dialysis) 5. Recent myocardial infarction, stroke, heart failure (in preceding 30 days) 6. Recent injurious fall requiring hospitalisation (in preceding 30 days) 7. Concomitant major illness / comorbidity that may result in death in the next 6 months 8. Participation in another study that is likely to affect BP levels 9. Inability to provide consent due to cognitive impairment.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hôpital du Sacré-Coeur de Montréal
Montreal, Quebec, H4J1C5, Canada
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Other studies related to the condition(s) this trial covers.
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