Comparing techniques for placing IV lines in patients with difficult veins

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to compare the effectiveness of ultrasound-guided and infrared illumination techniques against the standard method for peripheral venous catheterization (PVC) in patients with difficult venous access. The research will assess the success rates of these techniques on the first attempt, utilizing the A-DIVA clinical score to predict outcomes. Conducted at Poitiers Hospital, the study focuses on patients scheduled for CT scans who require a peripheral venous line. The goal is to identify the most effective method to enhance patient comfort and care.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients aged 18 or over
* Patient with a CT scan appointment and a medical prescription requiring a peripheral venous line.
* Patient with an A-DIVA score greater than or equal to 2.
* Patient able and willing to comply with all study procedures.
* Patient covered by a social security scheme or covered through a third party.
* Patients who have given their free and informed written consent following clear and fair information about the study.

Exclusion Criteria:

* Patient with a contraindication to VVP insertion:
* Arm with arteriovenous fistula
* Limb with an orthopaedic or vascular prosthesis
* Previous mastectomy, axillary lymph node dissection or homolateral radiotherapy of the arm
* Paralysed limb
* Presence of haematomas or puncture site wounds
* Limb with phlebitis or infection
* Patients already included in the study
* Persons benefiting from enhanced protection, i.e. minors, persons deprived of their liberty by a judicial or administrative decision, persons staying in a health or social establishment, pregnant or breast-feeding women, adults under legal protection and patients in emergency situations.

Where it's running

• Poitiers Hospital
  Poitiers, France Recruiting

Study contacts

• Study coordinator: Guillaume DAVY, Master
• Email: guillaume.davy@chu-poitiers.fr
• Phone: +33516604285

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.