Effectiveness of a Zinc Oxide Adhesive Securement Device in the Fixation of Midline and Peripherally Inserted Central Catheters in Hospitalized Adult Patients
Recruiting
N/A
Interventional Study
Vascular Access Complication
Skin and Subcutaneous Tissue Disorders
Phlebitis
Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 400 (estimated)
- Sponsor
- Hospital Arnau de Vilanova · Other
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About This Trial
Study in which a zinc oxide fixation device (a product that can help protect the skin) for catheters (polyurethane tubes inserted into a vein) will be tested to reduce catheter-related complications: catheter displacement, skin complications, phlebitis and pain..
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* requiring cannulation of a midline catheter or a PICC
* who accepted and signed the informed consent voluntarily
* with an inpatient unit admission of minimum 7 days
Exclusion Criteria:
\- patients with a known allergy to zinc oxide
Contacts