Can a Light-Guided device make arterial sticks easier?
NCT ID NCT07765199
First seen Aug 14, 2026 · Last updated Aug 14, 2026
Summary
This study tests whether a new device called Blood'up can help locate the radial artery in the wrist better than the traditional method of feeling for the pulse. Healthy volunteers will have arterial blood samples taken from both wrists, one using the device and the other using manual palpation, to compare success rates. The study also includes a group where low blood pressure is simulated with a blood pressure cuff, to see if the device helps when the pulse is harder to feel. The goal is to see if this technology could reduce the number of needle sticks needed and improve patient comfort.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Blood'up device (a non-invasive ultrasound-based device that projects a light signal to locate the radial artery) compared with manual palpation
- What this could lead to
- If effective, this device could help healthcare workers find arteries more easily, especially in patients with low blood pressure, reducing pain and complications from repeated punctures.
- What could go wrong
- This is a small pilot study in healthy volunteers, so results may not apply to real patients. The device is still under development and may not improve success rates as hoped.
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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About 32 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2027
An estimate. End dates often move.
- 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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Accepted
You do not need to have the condition being studied to take part.
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: * Participant who has agreed to take part in the study * No history of cardiovascular disease and a positive Allen test (the Allen test confirms the presence of collateral circulation between the radial and ulnar arteries) * Age ≥ 18 years * Body mass index (BMI) \< 30 kg/m² Exclusion Criteria: * Raynaud's syndrome/disease * Damaged or injured skin at the puncture site or at the Blood'Up device contact area * Upper limb amputation * Contraindication to arterial puncture in one or both upper limbs (e.g., skin lesion, lymph node dissection, etc.) * Contraindication to extrinsic arterial compression * Therapeutic anticoagulation * Known allergy to thermoplastic (ABS) * Known allergy to EMLA patch (lidocaine or prilocaine) * Pregnant or breastfeeding women
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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CHU Orléans
Orléans, 45067, France
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