Catheter Dislocation and the Influence of Different Catheter Fixation in Pediatric Patients
NCT ID: NCT05799989
Last Updated: 2023-06-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
100 participants
OBSERVATIONAL
2023-06-01
2024-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Surgical fixation
Pediatric patients with intravenous and/or intraarterial catheter in situ secured with surgical fixation
Surgical fixation
Pediatric patients with intravenous and/or intraarterial catheter in situ secured with surgical fixation
Atraumatic fixation
Pediatric patients with intravenous and/or intraarterial catheter in situ secured with surgical fixation
Atraumatic fixation
Pediatric patients with intravenous and/or intraarterial catheter in situ secured with atraumatic fixation
Interventions
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Surgical fixation
Pediatric patients with intravenous and/or intraarterial catheter in situ secured with surgical fixation
Atraumatic fixation
Pediatric patients with intravenous and/or intraarterial catheter in situ secured with atraumatic fixation
Eligibility Criteria
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Inclusion Criteria
* estimated length of catheter left in place longer than 72 hours
Exclusion Criteria
* impossible patient´s evaluation after catheter insertion
19 Years
ALL
No
Sponsors
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Masaryk University
OTHER
Brno University Hospital
OTHER
Responsible Party
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Petr Štourač, MD
Clinical Professor
Principal Investigators
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Petr Stourac, prof. MD., Ph.D., MBA
Role: STUDY_CHAIR
Department of paediatric anaesthesia and intensive care medicine
Locations
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Brno University Hospital - Academic Centre for Malignant Hyperthermia of Masaryk University Brno
Brno, South Moravian, Czechia
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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KDAR FIXATION 2023
Identifier Type: -
Identifier Source: org_study_id
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