Evaluating catheter fixation methods in pediatric patients
Catheter Dislocation and the Influence of Different Catheter Fixation in Pediatric Patients: Prospective Observational Trial
This study tests which method of securing catheters works better for kids who need them for more than three days, to see if it helps prevent problems like dislocation.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | N/A to 19 Years |
| Sex | All |
| Sponsor | Brno University Hospital Academic / other |
| Locations | 1 site (Brno, South Moravian Region) |
| Trial ID | NCT05799989 on ClinicalTrials.gov |
What this trial studies
This observational study investigates the effectiveness of different catheter fixation methods in pediatric patients who require intravenous or intra-arterial catheters for more than 72 hours. It compares traditional surgical fixation to newer atraumatic fixation techniques, assessing demographic data and complications associated with each method. The goal is to determine which fixation method better prevents catheter dislocation and related complications in this vulnerable population.
Who should consider this trial
Good fit: Ideal candidates are pediatric patients with intravenous or intra-arterial catheters expected to remain in place for longer than 72 hours.
Not a fit: Patients whose catheters are expected to be in place for less than 72 hours or who cannot be evaluated post-insertion may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved catheter management practices, reducing complications and enhancing patient safety in pediatric care.
How similar studies have performed: While there is ongoing research in catheter fixation methods, this specific comparison of surgical versus atraumatic fixation in pediatric patients is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * pediatric patients with intravenous/intraarterial catheter secured at Departement of pediatric anesthesiology and intensive care medicine * estimated length of catheter left in place longer than 72 hours Exclusion Criteria: * estimated length of catheter left in place shorter than 72 hours * impossible patient´s evaluation after catheter insertion
Where this trial is running
Brno, South Moravian Region
- Brno University Hospital - Academic Centre for Malignant Hyperthermia of Masaryk University Brno — Brno, South Moravian Region, Czechia (Recruiting)
Study contacts
- Study coordinator: Jozef UO Klučka, assoc.prof.MD., Ph.D.
- Email: klucka.jozef@fnbrno.cz
- Phone: +420532234696
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.