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Not yet recruiting NCT07315711

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

— Observational Peripheral Vascular Access in Pediatric Patients Peptic Ulcer Cataract Crohn's Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Peripheral Vascular Access in Pediatric Patients, Peptic Ulcer, Cataract, Crohn's Disease. Basic parameters: 0 Days — 18 Days · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

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

Overview

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.

Primary outcome measures

  • The time to establish peripheral vascular access [Time frame: pre-intervention/procedure/surgery]
  • number of attempts [Time frame: pre-intervention/procedure/surgery]
Secondary outcome measures (1)
  • number of interventions (each new skin entry of the needle) [Time frame: pre-intervention/procedure/surgery]

Eligibility criteria

Inclusion criteria

  • 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

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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Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-control

Study locations

Turkey (Türkiye) · 6 centers
  • Erciyes University Hospital — Kayseri
  • Erciyes University Hospital — Kayseri
  • Erciyes University Hospital — Kayseri
  • Erciyes University Hospital — Kayseri
  • Erciyes University Hospital — Kayseri
  • Erciyes University Hospital — Kayseri

Identifiers

NCT: NCT07315711 · 2025/454

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗