Brain-Guided blood pressure during surgery may cut risks
NCT ID NCT05308290
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This pilot study tested whether keeping blood pressure within a range that ensures good blood flow to the brain during surgery is feasible and safe compared to usual care. Researchers enrolled 27 older adults having hip, knee, or lung surgery. They measured how often blood pressure fell outside the brain's comfort zone and checked for complications like heart attack, stroke, and delirium.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this approach could reduce complications like delirium and stroke after surgery in older patients.
- What could go wrong
- This is a very small pilot study (27 participants) with no phase, so results may not apply broadly. The intervention is a blood pressure management strategy, not a drug, so benefits may be modest.
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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27 people
The number who actually took part.
- Started
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Jan 2023
- 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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60 to 100 years
- 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: * planned hip or knee surgery (either for fracture or elective) or lung surgery * age ≥60 * ambulatory at baseline * expected duration of surgery \> 90 minutes Exclusion Criteria: * Planned concurrent surgery * Allergy to adhesive tape * Short Blessed Test score \>20 * Clinical diagnosis of dementia * Opinion of either the anesthesiologist or surgeon that the patient is not appropriate.
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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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The Johns Hopkins University
Baltimore, Maryland, 21287, United States
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