Human Milk Oligosaccharides (HMOs) Profiles and Growth Indicators of Infants Aged 0-4 Months
NCT ID: NCT04515264
Last Updated: 2022-08-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
120 participants
OBSERVATIONAL
2021-08-01
2022-04-22
Brief Summary
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Detailed Description
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The study will be conduct in Government \& Private Hospital in Jakarta between Juli - December 2020. Based on sample size calculation, the total minimal samples are 120 samples. Subjects recruitment will be based on nonprobabilistic consecutive sampling to post partum inpatient mothers in Government \& Private Hospital in Jakarta between Juli - December 2020.
Study forms consist of study information, informed consent, screening form, baseline data, follow up form and laboratory result form. The tools requirements are among others Seca 728 electronic infant scale, Anthropometry Plus (AnthroPlus) Software, World Health Organization (WHO) growth velocity chart, Questionnaires, Thermometer, 15 mL polypropylene tube, Disposable gloves and vacuum bag with dry ice. The specimens obtain for this study are 15 mL venous blood for genotyping and 10 mL breast milk (0, 2, 4 month).
After obtaining clearance from Ethical Committee of the Faculty of Medicine University of Indonesia, the post partum mothers will be presented with Form A (study information form). Patients will be informed about the aim, benefits and procedures of the study. If patients agree, she will have to sign the informed consent (Form B).
Study phases consists of
1. screening : description of the aims, benefits and procedures of the study, filling the informed consent, screening based on inclusion and exclusion criteria.
2. Data collection :
* Interview. Interview will be done to fill information in Form C and D.
* Subjects selected during the screening visit will follow a 4 month study. Primary and secondary outcomes will be measured at 0, 2, 4 months (visit 1-2-3).
3. Data analysis :
1. All data will be edited, coded and entry to the computer. The Statistical Package for the Social Sciences (SPSS) for windows version 20.0 will be use for data analyzing.
2. Univariate analysis will be conduct to know the distribution of each variables. Test of normality of the data will be perform with Kolmogorov-Smirnov test at the significance level p\>0.05 as normally distributed data. The continuous data will be present as mean ± standard deviation and for categorical data in n (%) for normally distributed data and geometric mean ± standard deviation forn non-normally distributed data.
3. For bivariate analysis, Pearson correlation test will be performed if the data is normally distributed or Spearman Rank test if the data is non-normally distributed. Reference for rho value show in Table 3.3.
4. Multivariate analysis will be conduct by linear regression model.
Conditions
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Study Design
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OTHER
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Age of 18-45 year at the time of delivery
* Willing to breastfed at least up to 4 month
* Singleton birth
Exclusion Criteria
* Type 1 or 2 diabetes before or during pregnancy
* Presenting conditions that contraindicate breastfeeding
* Smoking
* Infant :
* Congenital illness or malformation that could affect growth
* Infants received water or any other food besides breast milk
2 Weeks
4 Months
ALL
Yes
Sponsors
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Wyeth nutrition indonesia
UNKNOWN
Indonesia University
OTHER
Responsible Party
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Verawati Sudarma
Principal Investigator
Principal Investigators
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Verawati Sudarma, Master
Role: PRINCIPAL_INVESTIGATOR
Indonesia University
Locations
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Universitas Indonesia
Jakarta, DKI Jakarta, Indonesia
Countries
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Other Identifiers
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HMOs Indonesia 1
Identifier Type: -
Identifier Source: org_study_id
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