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The study was designed as a prospective, observational study. Pediatric patients under 18 years of age scheduled for peripheral vascular access placement during day-case surgery or non-operating room anesthesia (NORA) will be included. The primary outcomes include time to successful vascular access, number of attempts, and number of interventions (defined as each new skin entry of the needle). These outcomes will be compared between two groups: those who receive vascular access with the aid of a vascular imaging device and those in whom such a device is not used.
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Inclusion criteria
Patients requiring peripheral vascular access (those with a need for intravenous access)
Patients whose parent or legal guardian can provide written informed consent
Patients suitable for vascular access using a vascular imaging device
Exclusion criteria
Patients requiring emergency surgery or urgent intervention
Patients whose parent or legal guardian cannot provide informed consent
Patients with local extremity problems such as infection, edema, or wound that prevent peripheral vascular access placement
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500 participants in 2 patient groups
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Central trial contact
RECEP AKSU, PROFESSOR; Sibel Seckin Pehlivan, Assistant Professor
Data sourced from clinicaltrials.gov
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