Crohn'sNot yet recruiting

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

Observational · No treatment assigned · 6 sites · Sibel Seçkin Pehlivan

Official record & contacts on ClinicalTrials.gov ↗

In plain English

What this trial is testing

Condition(s) listed: Peripheral Vascular Access in Pediatric Patients, Peptic Ulcer and Cataract. This is an observational study: researchers collect information (for example questionnaires, samples, or scans) but the study does not assign a treatment.

Who can join

Ages 0 Days to 18 Days
Any sex

Some of the main requirements, copied from the record:

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

Plus 1 more requirement(s). There are also 3 reasons someone might not be able to join (exclusion criteria). Only the trial team can confirm whether you qualify.

What's involved

About 500 participants are expected to take part.
Start date: 2025-12-01 (planned).
Main results expected around 2027-12-01 (estimate from the record).
6 study sites listed in Turkey (Türkiye).

Main thing being measured

The time to establish peripheral vascular access (pre-intervention/procedure/surgery)

In the researchers’ words

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.

This is a short automatic summary built from the official record. A fuller plain-English card is coming; until then, please read the official record.

Questions to ask your doctor and the trial team

Am I likely to qualify, given my health history?
What would I have to do, and how often would I need to visit?
Could I get a placebo? What happens to my current treatment?
What are the possible risks and benefits?
Are travel or other costs covered?
What happens after the trial ends?

Official details

Status	Not yet recruiting
Phase	Observational
Study type	Observational
Conditions	Peripheral Vascular Access in Pediatric Patients; Peptic Ulcer; Cataract; Crohn's Disease
Lead sponsor	Sibel Seçkin Pehlivan
Enrollment	500 (estimated)
Start date	2025-12-01
Primary completion (est.)	2027-12-01
First posted	2026-01-02
Last updated	2026-01-02
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
ClinicalTrials.gov ID	NCT07315711

Interventions

None listed

Full eligibility criteria (from the record)

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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Locations (6)

Site	City	Country
Erciyes University Hospital	Kayseri	Turkey (Türkiye)
Erciyes University Hospital	Kayseri	Turkey (Türkiye)
Erciyes University Hospital	Kayseri	Turkey (Türkiye)
Erciyes University Hospital	Kayseri	Turkey (Türkiye)
Erciyes University Hospital	Kayseri	Turkey (Türkiye)
Erciyes University Hospital	Kayseri, Kayseri̇	Turkey (Türkiye)

For contacts at each site, use the official record.

Information only, not medical advice. Talk to your doctor and the trial team before making any decision about a clinical trial.