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NCT07765199
Blood'up Device Versus Manual Palpation for Arterial Puncture in Healthy Volunteers: A Pilot Randomized Study Under Normal and Simulated Hypotension
Conditions: Arterial Puncture, Radial Artery Injury, Hypotension, Healthy
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: Yes
Phase: NA
Enrollment: 32
Sponsor: Centre Hospitalier Régional d'Orléans
Location: CHU Orléans Orléans
Summary
Arterial puncture is a common procedure in the management of hospitalized patients. It is most often performed at the level of the radial artery and allows arterial blood gas analysis.
The success rate of arterial puncture varies widely in the literature. This procedure is moderately painful and may cause significant discomfort, particularly in cases of repeated attempts. First-attempt success is therefore important to reduce both pain and the risk of local complications associated with multiple punctures.
In routine practice, arterial puncture is performed using manual palpation of the radial artery, typically by a trained nurse. In case of failure, a physician may attempt the procedure, often using ultrasound guidance. However, ultrasound is not routinely used and requires specific training and organizational protocols for nurse use.
In hypotensive conditions, such as shock, the radial pulse may become difficult to palpate, making arterial puncture more challenging when using conventional techniques.
The Blood'up device (Arterya, Hérouville, France) is a non-invasive device currently under development that assists in arterial localization. It is applied to the wrist and projects a light signal indicating the position of the artery. This localization is based on ultrasound technology using piezoelectric sensors integrated into the device.
The aim of this study is to evaluate the effectiveness of the Blood'up device for radial artery localization in healthy volunteers, both under physiological conditions (normal blood pressure) and under simulated hypotensive conditions.
Eligibility Criteria
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
Source: ClinicalTrials.gov (NCT07765199). StuddyBuddy aggregates publicly available trial information.