Neonatal pain. Acute pain
Conditions
Interventions
Intervention 1: For the familiar odor group, familiarization will be performed the night before blood sampling and neonates will be exposed to the vanillin odor during the painful procedure. In this g
Prevention
Treatment - Drugs
Control group: no intervention
For neonates in the unfamiliar group, the familiarization will not be carried out but blood sampling will be done in the presence of the vanillin odor 0/64%.
For the familiar odor group, familiarization will be performed the night before blood sampling and neonates will be exposed to the vanillin odor during the painful procedure. In this group, a sterile
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
No minimum to 1 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Age 1-7 days, 37-42 weeks of gestational age at birth, no neurologic, cardiologic or respiratory impairments or congenital anomalies Exclusion criteria: restlessness before the procedure, receiving sedatives or analgesics for 24 hours before the procedure, neonates in whom, the first needling for blood sampling was not successful
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| O2 Saturation. Timepoint: two minutes prior to sampling, after inserting and removing the needle. Method of measurement: pulse oximeter.;Heart Rate. Timepoint: two minutes prior to sampling, after inserting and removing the needle. Method of measurement: Pulse oximeter. | — |
Secondary
| Measure | Time frame |
|---|---|
| Crying duration. Timepoint: from onset until a crying free interval of more than five seconds. Method of measurement: voice recording. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAkram sadat Sadat Hoseini
Tehran University of Medical Sciences
Outcome results
None listed