New finger device could replace painful blood pressure needles for kids
NCT ID NCT04817137
First seen Jun 25, 2026 · Last updated Jul 24, 2026 · Updated 3 times
Summary
This study tested a non-invasive device worn on the finger to continuously measure blood pressure in children during surgery. Researchers compared its readings to those from an arterial line, the standard method that requires a needle. If proven accurate, this device could offer a safer, less painful way to monitor blood pressure in young patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- CareTaker PDA Device
- What this could lead to
- If accurate, this device could replace invasive arterial lines for blood pressure monitoring in children, making it safer and less painful.
- What could go wrong
- This is a small, early validation study with only 35 children. The device may not be accurate enough for all patients or situations.
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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35 people
The number who actually took part.
- Started
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May 2021
- Finished
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Jul 2023
- 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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2 to 17 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: * Plan to receive an invasive arterial blood pressure monitor as part of their anesthesia care plan at the BCH Longwood campus Exclusion Criteria: * Patients with vascular or congenital heart disease known to affect large and small arteries * Patients who declined to participate.
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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
-
Boston Children's Hopsital
Boston, Massachusetts, 02115, United States
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