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Clinical Trials/NL-OMON38895
NL-OMON38895CompletedNot Applicable

Validity and reliability of test weighing (weighing before and after a feed) in term and preterm neonates according to a standardized validated test weighing technique in clinical practice. - Reliability of test weighing in neonates

IJssellandziekenhuis0 sites45 target enrollmentStarted: TBDLast updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
45
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
2 to 11 (—)

Inclusion Criteria

  • •Infants, admitted to the neonatal ward of the IJsselland Hospital, a general hospital in the Netherlands.
  • •The infants meet the following criteria: postconceptional age on day of study between 34 and 44 weeks, with or without feeding tube, iv drip and infusion splint, monitor lead wires.
  • •The infants are bottle fed mothermilk or formula with volumes at least 10 ml

Exclusion Criteria

  • •Clinically unstable neonates, assessment of clinical stability by the attending pediatrician.
  • •Neonates who required continuous connection to monitors
  • •Neonates who are not able to drink from bottle
  • •Exclusively breastfed neonates

Investigators

Sponsor
IJssellandziekenhuis

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