Intensity of pain During Venous Blood sampling in Preterm Neonates.
Conditions
Interventions
Intervention 1: Intervention group: Sucrose group: Infants who receive 24%sucrose from 2 minutes before injection to 2 minutes after injection. In this group, the standard 24%sucrose, 0/2 ml / kg is
Sponsors
Babol University of Medical Sciences
Eligibility
Sex/Gender
All
Age
1 Days to 28 Days
Inclusion criteria
Inclusion criteria: Term infants with a gestational age of 42-37 weeks Stability of vital signs before sampling No congenital or genetic abnormalities Non-use of drugs, antidepressants and anticonvulsants by the mother during pregnancy No surgery and receiving anesthesia and anesthesia drugs Lack of intubation
Exclusion criteria
Exclusion criteria: Abnormalities in the head and skull such as cleft lip and palate and atrial fibrillation Infants who experience more than grade II intraventricular hemorrhage during the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intensity of pain during venous blood sampling in preterm infants. Timepoint: 2 minutes before, during and 2 minutes after blood sampling. Method of measurement: Neonatal Infant Pain Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Infant heart rate changes 15 minutes before, during and 15 minutes after intravenous sampling. Timepoint: 2 minutes before, during and 2 minutes after intravenous sampling. Method of measurement: Cardiorespiratory monitoring device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAli Zabihi
Babol University of Medical Sciences
Outcome results
None listed