Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06905119

Digital Transformation of Continuity of Care for Peripherally Inserted Central Catheters: SpadCare Experience

Led by Fundacion Miguel Servet · Updated on 2025-09-12

201

Participants Needed

1

Research Sites

169 weeks

Total Duration

On this page

Sponsors

F

Fundacion Miguel Servet

Lead Sponsor

U

Universidad Pública de Navarra

Collaborating Sponsor

AI-Summary

What this Trial Is About

The study focuses on patients who require outpatient infusion of therapy ("Infusions, Intravenous"\[Mesh\]) "Administration, Intravenous"\[Mesh\] ("Home Infusion Therapy"\[Mesh\]) "Parenteral Nutrition, Home"\[Mesh\] via a peripherally inserted central catheter (PICC) ("Central Venous Catheters"\[MeSH\] "Catheterization, Central Venous"\[MeSH\] "Catheterization, Peripheral" \[MeSH\] "Vascular Access Devices"\[Mesh\] )

CONDITIONS

Official Title

Digital Transformation of Continuity of Care for Peripherally Inserted Central Catheters: SpadCare Experience

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients >18 years.
  • Sign the informed consent form.
  • Have a Smartphone and accept the use of the APP.
  • Patient with a PICC inserted by the Infusion and Vascular Access Team of the University Hospital of Navarra and with a planned use of at least one month.
Not Eligible

You will not qualify if you...

  • Patients with limitations in the use of digital resources or lack of Smartphone.
  • Patients who do not want to install the APP on their Smartphone.
  • Patients who do not authorize access to their Computerized Medical Record (HCI).

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hospital Universitario de Navarra

Pamplona, Navarre, Spain, 31003

Actively Recruiting

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Research Team

M

María Inés Corcuera Martínez MI Corcuera Martínez, RN-PhD(c)

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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