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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03849248
Other study ID # SBS-2018-0527
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 24, 2019
Est. completion date March 1, 2023

Study information

Verified date April 2022
Source American University of Beirut Medical Center
Contact Saadieh Masri, RN
Phone 01374444
Email sm52@aub.edu.lb
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To study the effect of maternal scent on the oral feeding, behavior and stress level of premature infants hospitalized in the Neonatal intensive care unit and to assess its potential effect on their development at 18 to 24 months.


Description:

Premature infants develop their sense of smell very early in the womb. After birth infants can recognize and distinguish the odor of their mother from their father and others. Premature infants are capable of smelling and they experience less pain and agitation when they smell their mother's milk; studies have shown that premature infants have better sucking and feeding, and they may go home earlier when they are exposed to the odor of breast milk. It is not known whether the same will happen if preterm infants are exposed to their mother's smell rather than the smell of the maternal milk.


Recruitment information / eligibility

Status Recruiting
Enrollment 132
Est. completion date March 1, 2023
Est. primary completion date March 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A to 10 Days
Eligibility Inclusion Criteria: - Mother of a baby who was born premature before completing 36 weeks of pregnancy - Baby between ages of 5-10 days - Medically stable baby - Baby already began feeding by mouth or by feeding tube Exclusion Criteria: - Medically unstable baby born after 36 weeks of gestation.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Maternal scent cloth
The babies assigned to the intervention group will have a cloth with their mother's scent on it placed under their heads.

Locations

Country Name City State
Lebanon American University of Beirut Beirut

Sponsors (1)

Lead Sponsor Collaborator
American University of Beirut Medical Center

Country where clinical trial is conducted

Lebanon, 

Outcome

Type Measure Description Time frame Safety issue
Primary Salivary cortisol level The saliva will be collected from infant mouth after enrollment the first day before placing the scented cloth under the infant's head and the second after the exposure to the second cloth.
Levels will be compared before and after and between groups.
Two years
Secondary Physiological parameters: Heart rate and respiratory rate Infant's heart rate and respiratory rates will be measured. Two years
Secondary Achievement of oral feeding The number of days to reach oral feeding of all prescribed feeds will be recorded from the infant medical record, this will be compared between the intervention and control group. Two years
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