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Recruiting NCT05878483

NCT05878483 Autonomous Blood Drawing Optimization and Performance Testing

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Clinical Trial Summary
NCT ID NCT05878483
Status Recruiting
Phase
Sponsor Vitestro B.V.
Condition Venipuncture
Study Type INTERVENTIONAL
Enrollment 44,658 participants
Start Date 2023-07-21
Primary Completion 2029-12-31

Trial Parameters

Condition Venipuncture
Sponsor Vitestro B.V.
Study Type INTERVENTIONAL
Phase N/A
Enrollment 44,658
Sex ALL
Min Age 16 Years
Max Age N/A
Start Date 2023-07-21
Completion 2029-12-31
Interventions
Venipuncture Device (VD)

Eligibility Fast-Check

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Brief Summary

The purpose of this pre-market clinical study is to evaluate the performance (efficacy) and safety of an autonomous blood drawing device (Venipuncture Device). The study consists of several phases (A, B1, B2, C1, C2, C3, 0). Phase B1 is a confirmatory, Pivotal Clinical Study, required for regulatory approval, in which non-inferiority should be demonstrated in comparison to manual blood drawing. Phases A, B2, B3, C1, C2, C3 are all exploratory studies, in which the technology and usability is further improved and tested. Phase 0 is an exploratory study for non-invasive technology testing (for example for improvement of ultrasound detection). The study locations are outpatient blood drawing departments, in which patients are included as subjects. Additionally, in Phase A and C1, a small number of volunteers can be included in a non-hospital site (Vitestro Site).

Eligibility Criteria

Inclusion Criteria: • Age ≥16 years. Exclusion Criteria: * Unable to follow instructions, due to mental disability and/or incapacity * Unable to use device correctly due to physical impairment or disability (for example a patient with severe contractures or deformities) * No venipuncture possible in cubital fossa of both arms (for example: after amputation of both arms) * No venipuncture possible in cubital fossa due to contra-indications in both arms (for example: tattoos in both arms) * Incapacitated persons * Pregnant or breast-feeding The following contra-indications / exclusion criteria are respected per arm: * Arteriovenous fistula or vascular graft * Paretic or paralyzed arm (e.g. after stroke or trauma) * Infected skin in cubital fossa (for example: erysipelas or cellulitis) * Mastectomy side, axillary lymph node excised * Healed skin burns in cubital fossa * Edema in cubital fossa * Extensive scarring in cubital fossa * Hematoma in cubital fossa * Tattoos in cubital fossa In c

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