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Preterm Neonatal Feeding Protocol Comparing Feed Administration Time

Oregon Health & Science University (OHSU) logo

Oregon Health & Science University (OHSU)

Status

Completed

Conditions

Feeding Intolerance

Treatments

Other: Length of time for feed administration

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Doctors have tried many different methods of feeding to try to decrease feeding intolerance in preterm babies so that they spend less time receiving liquid nutrition and have fewer problems with feeding intolerance.

The purpose of this study is to test two different methods of feeding preterm babies in the hopes of identifying a method that will decrease some of the feeding intolerance that can occur when feeding premature babies.

Enrollment

136 patients

Sex

All

Ages

Under 32 weeks old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Any infant born at OHSU or transferred in from another facility whose birthweight is greater than 500 grams and less than 1500 grams, and whose gestational age is less than 32 weeks.

Exclusion criteria

  • Any infant who has major anomalies including but not limited to *gastroschisis

    • omphalocele
    • bowel obstruction or atresia
    • tracheo-esophageal fistula
    • Hirschsprung's Disease
    • congenital diaphragmatic hernia
    • congenital heart disease and other major syndromes
    • infants who have started enteral feeds prior to entering the study
  • Any infant whose birth weight is greater than or equal to 1500 grams or less than 500 grams

  • Any infant whose gestational age is greater than 32 weeks.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

136 participants in 2 patient groups

Group 1 Bolus Feeds
Active Comparator group
Description:
This group will receive feeds administered by bolus method over no more than 30 minutes per feed.
Treatment:
Other: Length of time for feed administration
Group 2- Slow Infusion Feeds
Experimental group
Description:
This group will receive feeds administered by slow infusion over pump for 2 hours.
Treatment:
Other: Length of time for feed administration

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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