Topical application of coconut oil to improve skin condition in very preterm infants- a pilot randomised controlled trial.
Not Applicable
Completed
- Conditions
- skin integrityLate onset sepsispreterm birthSkin - Dermatological conditionsReproductive Health and Childbirth - Complications of newbornInfection - Studies of infection and infectious agents
- Registration Number
- ACTRN12616000042448
- Lead Sponsor
- King Edward Memorial Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 72
Inclusion Criteria
(1) Gestation <30 weeks, (2) Postnatal age <24 hours, (3) Informed parental consent
Exclusion Criteria
(1) Presence of major congenital malformation/s requiring surgery, (2) Congenital skin abnormality or signs of skin infection, (3) life-threatening illness during the first 24h of life (as certified by the consulting physician)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Proportion of children with improvement in skin integrity<br> as assessed by the Neonatal skin condition scale (NSCS)<br>[ 3 weeks of life];Incidence of local skin irritation and infection as a composite out come and will be assessed as per guidelines given in Neonatal Skin condition scoring(NSCS) as adopted by<br>Association of Women’s Health, Obstetric and Neonatal Nurses (AWHONN).<br>REFERENCE<br>AWHONN. Neonatal Skin Care: Evidence-Based Clinical Practice Guideline 3rd ed. Washington USA: Johnson & Johnson; 2007.[Till end of the three week intervention period];Feasibility of the coconut oil application to the enrolled infants as per study protocol<br>.Measured as the proportion of preterm infants in which topical coconut oil could be applied successfully for three weeks.[End of three weeks of intervention]
- Secondary Outcome Measures
Name Time Method