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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04382989
Other study ID # MPS-2017
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 15, 2017
Est. completion date April 30, 2020

Study information

Verified date June 2020
Source Vilnius University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims for characterization of different maternal, infant and environmental factors (e.g. maternal age, pregnancy duration, lactation period, baby gender, circadian rhythm, Holder pasteurisation, etc.) that influence human milk composition.


Description:

The study consists of three parts. In the first part the investigators aim to evaluate human milk macronutrient composition depending on the time after delivery and pregnancy duration.

In the second part the investigators aim to evaluate the circadian variation of human milk macronutrient and energy content depending on pregnancy duration.

In the third part the investigators aim to evaluate the influence of Holder pasteurisation on human milk macronutrient, metabolome and bioactive protein (lysozyme and lactoferrin) content.


Recruitment information / eligibility

Status Completed
Enrollment 174
Est. completion date April 30, 2020
Est. primary completion date April 30, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

having obtained informed consent; after a single-birth pregnancy; women who were not on a special diet; lactating mothers who could not breastfeed their newborns due to the baby's medical condition (either prematurity or disease) but who expressed milk.

-

Exclusion Criteria:

breastfeeding mothers; history of maternal diabetes, hepatitis B or C, HIV, tuberculosis, mastitis, or oncological disease; drug addicted.

-

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Analysis of human milk composition by mid-infrared spectrophotometry
Analysis of human milk macronutrient content was performed by mid-infrared spectrophotometry using a Miris Human Milk Analyser. An immune-enzymatic ELISA assays were used to estimate lysozyme and lactoferrin concentrations in human milk.

Locations

Country Name City State
Lithuania Neonatal centre of Vilnius University Hospital Santaros Klinikos Vilnius

Sponsors (2)

Lead Sponsor Collaborator
Vilnius University University of Cagliari

Country where clinical trial is conducted

Lithuania, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quantification of total protein concentration in human milk Mid-infrared spectrophotometry from the 2nd week, up to 2 months after delivery
Secondary Quantification of total lipids and carbohydrate in human milk Mid-infrared spectrophotometry from the 2nd week, up to 2 months after delivery
Secondary Quantification of lactoferrin in human milk An immune-enzymatic ELISA assay 14-16 days after delivery
Secondary Quantification of lysozyme in human milk An immune-enzymatic ELISA assay 14-16 days after delivery
Secondary Human milk metabolome analysis Nuclear Magnetic Resonance (NMR) analysis 15-17 days after delivery
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