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Clinical trialNCT00728117CompletedInterventional

Feeding During Ibuprofen or Indomethacin Treatment of Preterm Infants

SponsorUniversity of California, San FranciscoEnrollment177Patent Ductus Arteriosus
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

We hypothesize that feeding preterm infants while they receive indomethacin or ibuprofen therapy for treatment of a patent ductus arteriosus will decrease the incidence of feeding intolerance and shorten the time period that infants need to tolerate full enteral nutrition. We also hypothesize that this intervention will minimize the alterations in intestinal permeability that occur with these drugs and will improve the infants' hemodynamic response to enteral nutrition
clinicaltrials.gov ↗

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

14 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • University of California San Francisco

    San Francisco, California, United States

  • Santa Clara Valley Medical Center

    San Jose, California, United States

  • Children'S Memorial Hospital-Northwestern University

    Chicago, Illinois, United States

  • North Shore University Health System, Northwestern University

    Evanston, Illinois, United States

  • Boston University-Boston Medical Center

    Boston, Massachusetts, United States

  • Children'S Hospital-Minneapolis

    Minneapolis, Minnesota, United States

  • Mayo Clinic

    Rochester, Minnesota, United States

  • Children'S Hospital-Saint Paul

    Saint Paul, Minnesota, United States

  • Atlantic Health Organization

    Morristown, New Jersey, United States

  • Columbia University

    New York, New York, United States

  • Case Western Reserve

    Cleveland, Ohio, United States

  • University of Pittsburgh

    Pittsburgh, Pennsylvania, United States

  • Vanderbilt University

    Nashville, Tennessee, United States

  • University of Virginia, Charlottesville

    Charlottesville, Virginia, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Jul 2008
Primary completion
31 Jul 2012
Completion
30 Sept 2012
Last update posted
9 Nov 2012
Registered enrollment
177
Registry id
NCT00728117
clinicaltrials.gov ↗

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 4 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.