Effect of pain relief methods blood sampling pain in newborns
Not Applicable
- Conditions
- Acute Pain.R52.0
- Registration Number
- IRCT201408029568N9
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Absence of asphyxia at birth based on infant records
Birth age of 2–28 days
Anticipated to have at least six heel sticks during the NICU hospitalization
No administration of sedatives relaxants, antiepileptic, or analgesic in 24 hours before every study session
Born to mothers with no history of addiction to substances
Not having any acute condition which required more critical care surgery
Not using of sedative, relaxants, antiepileptic, or analgesic drugs
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: before of intervention, during and after of intervention. Method of measurement: Premature Infant Pain Profile.
- Secondary Outcome Measures
Name Time Method Feasibility. Timepoint: After Intervention. Method of measurement: Questioning about simplicity and the applicability.