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NCT07315711Not yet recruiting

The Effect of Vascular Imaging Devices on Success Rates of Peripheral Vascular Access in Pediatric Patients

The Effect of Vascular Imaging Devices on the Success Rate of Peripheral Vascular Access in Pediatric Patients Undergoing Day-Case and Non-Operating Room Anesthesia Procedures

Source: ClinicalTrials.gov · Last updated 2 Jan 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
500 (estimated)
First submitted
10 Dec 2025
Start date
1 Dec 2025
Primary completion date
1 Dec 2027
Lead sponsor
Sibel Seçkin Pehlivan
NCT number
NCT07315711

What you commit to

  • Study type: Observational
  • Planned participants: 500
  • From 1 Dec 2025 to the primary completion date, 1 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients requiring emergency surgery or urgent intervention

Other illness

  • Patients with local extremity problems such as infection, edema, or wound that prevent peripheral vascular access placement

Other

  • Patients whose parent or legal guardian cannot provide informed consent
  • \-

Who the study is looking for

  • Pediatric patients aged 0-18 years scheduled for day-case surgery or non-operating room anesthesia (NORA)
    • 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

Age in the registry: 0 days to 18 days · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Erciyes University Hospital
Coordinator of this site? Confirm its status
KayseriTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.