Feeding Study in Premature Infants

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00681018

Enrollment

143

Registered

2008-05-20

Start date

2008-09-30

Completion date

2010-08-31

Last updated

2010-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Premature Infants

Keywords

premature, infants

Brief summary

To evaluate weight gain of preterm infants fed fortified human milk.

Interventions

OTHERLiquid human milk fortifier

Liquid human milk fortifier added to human milk

OTHERPowder human milk fortifier

Powder human milk fortifier added to human milk

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

SUPPORTIVE_CARE

Masking

QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender

ALL

Age

No minimum to 40 Days

Healthy volunteers

Yes

Inclusion criteria

* premature infant * birth weight less than/equal to 1250 g * exclusively breast fed

Exclusion criteria

* metabolic or chronic disease * major surgery * ventilator dependent

Design outcomes

Primary

Measure	Time frame
Weight gain	28 days

Secondary

Measure	Time frame
Feeding tolerance	28 days

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026