The Effect of Exposure to Maternal Human Milk Odor on Physiological State of Preterms.
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|ClinicalTrials.gov Identifier: NCT01012505|
Recruitment Status : Unknown
Verified November 2009 by Sheba Medical Center.
Recruitment status was: Not yet recruiting
First Posted : November 13, 2009
Last Update Posted : November 13, 2009
Mammalian fetal sensory development comes in an invariant series, with the tactile/kinesthetic and chemosensory systems the earliest functioning and responsive to stimulation, implicating the importance of these foundational sensory systems for later development. Olfaction is essential for neonatal behavioral adaptation in many mammals, including humans. Experiments show that newborns recognize, and are soothed by, the smell of amniotic fluid. Provision of the mother's smell with breast pads, handkerchiefs she has worn, breast milk on a cotton ball or cotton applicator, or other means of providing odor and taste input can facilitate recognition by the infant's mother at a later time and does not appear to be detrimental to the stability of the infant.
Provision of the odor and taste of the mother's milk has been shown to facilitate the infant's mouthing, sucking, arousal, and calming from irritability, especially in preparation for oral feeding. Using 24 hour monitor analysis and cortisol saliva measurements, we will provide quantitive analysis to the effect of smell.
|Condition or disease||Intervention/treatment|
|Health Preterm Infants With no Active Disease Human Milk Nutrition Incubator Stay||Other: adding pad with maternal milk in hte incubator|
|Study Type :||Observational|
|Estimated Enrollment :||20 participants|
|Official Title:||The Effect of Exposure to Maternal Human Milk Odor on Physiological State of Preterms.|
|Study Start Date :||December 2009|
20 preterm infants
20 preterm infants without active disease
Other: adding pad with maternal milk in hte incubator
2 days prior to intervention - recording infants data and taking saliva cortisol adding pad with maternal milk - during 2 days - recording infants data and taking saliva cortisol.
stopping intervention and for other 2 days recording infants data and taking saliva cortisol
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01012505
|Sheba medical center||Not yet recruiting|
|Ramat - Gan, Israel, 52621|
|Contact: Ayala Maayan-Metzger, Dr. 972-3-5302227 email@example.com|