Comparing the effect of sucrose taste, maternal breast milk odor and taste on the pain associated with venous blood sampling in neonate.
Conditions
Interventions
Intervention 1: Intervention group: In the milk odor intervention group, 2 cc of milk was poured into cotton balls and placed for 3 minutes before to 30 seconds, and 2 cc of normal saline was poured
Prevention
Intervention group: In the milk odor intervention group, 2 cc of milk was poured into cotton balls and placed for 3 minutes before to 30 seconds, and 2 cc of normal saline was poured into the baby's
Intervention group: In the group, the taste of sucrose, 2 cc sucrose 24%, is cast 3 minutes before the procedure in the front part of the baby's nose, and the cotton bullet stained with normal saline
Intervention group: In the breast milk taste group, 2-cc of maternal milk, by the syringe, is cast in the front of the baby's tongue 3 minutes before sampling, and the cotton ball covered with norma
Sponsors
Babol University of Medical Sciences
Eligibility
Sex/Gender
All
Age
2 Days to 30 Days
Inclusion criteria
Inclusion criteria: Babies with gestational age 37 to 42 weeks Sustained in terms of vital signs With Diagnosis of icter Complete vigilance
Exclusion criteria
Exclusion criteria: Fasting Receive nutrition within less than an hour before the intervention Get another painful procedure before the intervention Congenital abnormalities such as cleft palate, lumbar spine and atresia quan Refuse to continue to participate in research by parents Abnormalities in the head and skull Failure in venous blood sampling at first time
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: During intervention, After intervention. Method of measurement: Neonatal Infant Acute Pain Assessment Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Arterial oxygen saturation. Timepoint: Before intervention, during intervention, after intervention. Method of measurement: Mobile monitoring device.;Heart rate. Timepoint: Before intervention, during intervention, after intervention. Method of measurement: Mobile monitoring device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAsiyeh Modaresi
Babol University of Medical Sciences
Outcome results
None listed