Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00997854 · ClinicalTrials.gov registry record · NA

Preterm Neonatal Feeding Protocol Comparing Feed Administration Time

A NA study, sponsored by Oregon Health and Science University.

Completed
Registry status
NA
Development phase
136
Enrollment target

NCT00997854: Completed NA study, sponsored by Oregon Health and Science University.

NCT00997854 is a NA study that has completed, run by Oregon Health and Science University. The registered enrollment target is 136 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00997854, a NA study, has completed, sponsored by Oregon Health and Science University.

COMPLETED
Registry status
NA
Development phase
136 participants
Enrollment target

Study Summary

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.

Interventions

  • OTHER Length of time for feed administration

Trial Details

FieldValue
Enrollment Target 136 participants
Start Date 2009-10
Est. Completion 2010-10
Phase NA

What the finished NCT00997854 record still lists

NCT00997854 is an interventional study that assigns participants to a tested intervention. The registered 136 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 1 intervention - of which Length of time for feed administration is the first listed.

NCT00997854 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00997854 about?

NCT00997854 is a clinical study titled "Preterm Neonatal Feeding Protocol Comparing Feed Administration Time". 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 babie...

What is the current status of trial NCT00997854?

This trial is currently completed. It is a NA study. The enrollment target is 136 participants. The study started on 2009-10. Estimated completion is 2010-10.

What interventions are being tested in trial NCT00997854?

The interventions under investigation include: Length of time for feed administration (OTHER).

Who is sponsoring clinical trial NCT00997854?

This trial is sponsored by Oregon Health and Science University, which has 546 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00997854's enrollment target sits among peer trials

136 722nd of 2000 higher than 1,275 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01555892 · 136 participants · Phase 1

    Cytotoxic T-Lymphocytes for EBV-positive Lymphoma, GRALE

  • NCT03216525 · 136 participants · Phase 3

    Alvimopan Versus Placebo in Patients Undergoing Radical Cystectomy on an Enhanced Recovery Protocol

  • NCT04476901 · 136 participants · Phase 2

    Administration of Allogeneic-MSC in Patients With Non-Ischemic Dilated Cardiomyopathy

  • NCT04603898 · 136 participants · NA

    Oxalate Formation From Ascorbic Acid

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00997854, the US trial registry maintained by the National Library of Medicine. NCT00997854 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.