Quantification of breast milk intake of infants using the deuterium oxide dose-to-mother tehcnique (the BRINTA study)

Completed

• Conditions: gezondheid van zuigelingen; NA

• Registration Number: NL-OMON42042
• Lead Sponsor: Wageningen Universiteit

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 5

Inclusion Criteria

Female, apparently healthy
Lactating, either exclusively or partially during the entire study period of 2 weeks
Singleton and apparently healthy baby
Full term pregnancy (>37 weeks)

Exclusion Criteria

Participation in other studies
Kidney failure, congestive heart failure
Staying abroad for more than one week during the month preceding the study or planning to travel during the study period

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Average intake of breast milk over a 14-day period.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Maternal body composition and energy expenditure.</p><br>