Pain
Conditions
Interventions
Total sample of 15 preterm infants - design: cross-clinic trial
Group of 15 participants will receive 02 interventions during a blood collection through an arterial puncture.
It is a group and 02 cond
Sponsors
Universidade Federal de Alfenas
Hospital de Clínicas de Itajubá
Eligibility
Age
32 Weeks to 36 Weeks
Inclusion criteria
Inclusion criteria: Preterm infants of both sexes; gestational age between 32 to 36 weeks and six days; Hospitalization time longer than 24 hours; Weight greater than 1000g; Spontaneous ventilation or noninvasive ventilatory support; Medical prescription for arterial blood collection; Suspension of analgesic or sedative medication in the 12 hours prior to collection; Stability of vital signs considering the characteristics of the newborn.
Exclusion criteria
Exclusion criteria: Neonates diagnosed with heart disease; Genetic alterations and congenital anomalies; Immediate or mediated postoperative; Invasive and non-invasive ventilatory support of the Hood type.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Presentation of the expected outcome: It is expected to observe the effectiveness of the application of facilitated containment superior to winding, in reducing pain in premature infants during arterial puncture. This efficacy will be evaluated through the analysis of two tables, one that refers to pain assessment and the other referring to the developmental organization of premature newborns. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected | — |
Countries
Brazil
Contacts
Public ContactSandra dos Reis
Outcome results
None listed