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

Sponsor
Sibel Seçkin Pehlivan
Study ID
NCT07315711
Status
Not Yet Recruiting

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Conditions

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

Eligibility Criteria

Sex
ALL
Age
0 Days - 18 Days
Healthy Volunteers
Not accepted

Study Details

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.

Key Dates

First listed
Jan 2, 2026
Start date
Dec 1, 2025
Status verified
Dec 2025
Primary completion
Dec 1, 2027
Completion
Dec 1, 2027

Study Design

Enrollment
500 participants (estimated)

Arms

  • Arm: Intervention Group
    Pediatric patients undergoing peripheral vascular access with the use of a vascular imaging device. The intervention involves the application of real-time imaging guidance (e.g., near-infrared light or ultrasound) to facilitate successful and efficient cannulation.
  • Arm: Control Group
    Pediatric patients undergoing peripheral vascular access without the use of a vascular imaging device, relying on standard visual and palpation techniques.

Primary Outcome Measure

The time to establish peripheral vascular access [ Time Frame: pre-intervention/procedure/surgery ]

Central Contacts

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