Encounter for adjustment and management of vascular access device
Conditions
Interventions
This is a two-arm, double-blind, randomized controlled clinical trial. Experimental group: 30 peripherally inserted central venous catheter procedures will receive the modified measurement method, tha
Sponsors
Universidade Federal Fluminense
Programa de Pós-Graduação Mestrado Profissional em Enfermagem Assistencial
Eligibility
Age
No minimum to 28 Days
Inclusion criteria
Inclusion criteria: Peripherally inserted central catheter procedures in upper limbs; term newborns; preterm newborns; both sexes
Exclusion criteria
Exclusion criteria: Puncture site for catheter insertion other than in the upper limbs; insertion procedure performed in newborns with congenital anomalies of the venous network; newborns with coagulopathies; malformation in upper limbs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) Catheter placement in a central location using the experimental method. Assessed after radiographic examination, located in the superior vena cava or cavoatrial junction | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Reduction in the need for traction, handling or interventions after performing the peripherally inserted central catheter | — |
Countries
Brazil
Contacts
Public ContactRayhelle Cristiny Moura
Hospital Santa Juliana
Outcome results
None listed