N
← Back to Search
Sponsored

Accelerate Your Clinical Trial Recruitment

Reach thousands of high-intent patients matching your specific inclusion criteria.

Start Campaign
RECRUITING Not applicable ClinicalTrials.gov

Peripheral Venous Access Management by Radiologic Technologists in Radiodiagnostic Procedure

Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS • ClinicalTrials.gov ID: NCT07411430

Registry updated: 2026-10-14
Ad

Recruiting for Similar Conditions?

Sponsors are looking for patients like you. See if you qualify for compensated research studies.

Check Eligibility →

Description

The goal of this interventional study is to evaluate the impact of a structured training program on the ability of Radiologic Technologists (RTs) to safely and effectively perform peripheral venous access (PVA) placement for contrast media administration in a radiodiagnostic setting. The study focuses on adult patients undergoing contrast-enhanced imaging procedures and on Radiologic Technologists who have completed a competency-based theoretical and practical training program on peripheral venous access management. The main questions it aims to answer are: * Does a structured training program improve the theoretical knowledge and technical competencies of Radiologic Technologists in peripheral venous access placement? * What is the incidence of complications associated with peripheral venous access placement performed by trained Radiologic Technologists in routine clinical practice? * How do patients perceive the procedure in terms of pain, safety, procedural success, and overall satisfaction? Participants: * Radiologic Technologists will participate in a structured theoretical and practical training program focused on peripheral venous access placement for contrast media administration. * Radiologic Technologists will perform peripheral venous access placement during routine radiodiagnostic procedures following completion of the training. * Patients undergoing contrast-enhanced imaging will receive peripheral venous access placement performed by trained Radiologic Technologists and will complete questionnaires assessing pain, satisfaction, and perceived safety of the procedure.

Interventions

  • Structured Peripheral Venous Access Training Program (Other)
    The intervention consists of a structured, competency-based theoretical and practical training program designed to qualify Radiologic Technologists to independently perform peripheral venous access placement for contrast media administration. The program includes classroom-based education, supervised hands-on training, and on-the-job mentoring focused on venipuncture techniques, prevention and recognition of complications, and patient communication. Competency is achieved after completion of the training pathway and a minimum number of supervised procedures.

Eligibility criteria

Inclusion Criteria for Radiologic Technologists (RTs): * Voluntary participation and provision of written informed consent. * Completion of the structured theoretical and practical training program for peripheral venous access placement for contrast media administration. Inclusion Criteria for Patients: * Age ≥18 years * Provision of written informed consent. * Undergoing a contrast-enhanced CT or MRI examination requiring peripheral venous access placement for contrast media administration. Exclusion Criteria for Radiologic Technologists (RTs): \- No written informed consent. Exclusion Criteria for Patients: * Age \<18 years. * Severe cognitive impairment that precludes valid informed consent or completion of the patient survey. * No written informed consent. * Clinical conditions that make peripheral venous access placement complex or unsafe, as determined by the clinical team.

Conditions

Skill Development of Staff Clinical Practice Patient Satisfaction

Locations

  • Fondazione Policlinico Universitario Gemelli IRCCS — Roma, RM, Italy
Sponsored

Partner with Nurenyx

Showcase your study to thousands of motivated patients matching your criteria.

Learn More

Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record