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Clinical Trials/NL-OMON42042
NL-OMON42042
Completed
Not Applicable

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

Wageningen Universiteit0 sites5 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
gezondheid van zuigelingen
Sponsor
Wageningen Universiteit
Enrollment
5
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Eligibility Criteria

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

Outcomes

Primary Outcomes

Not specified

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