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Electrogastrography (EGC) in Premature Infants With Feeding Intolerance

Primary Purpose

Infant, Newborn, Diseases

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
metoclopramide
Sponsored by
National Center for Research Resources (NCRR)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infant, Newborn, Diseases focused on measuring Feeding intolerance, Infant, premature

Eligibility Criteria

1 Minute - 1 Month (Child)All SexesAccepts Healthy Volunteers

Inclusion: Premature infants. Absence of 1) infection, 2) congenital anomalies, 3) growth retardation

Sites / Locations

  • Children's Hospital of Philadelphia

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
January 16, 2001
Last Updated
June 23, 2005
Sponsor
National Center for Research Resources (NCRR)
Collaborators
Children's Hospital of Philadelphia
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1. Study Identification

Unique Protocol Identification Number
NCT00008736
Brief Title
Electrogastrography (EGC) in Premature Infants With Feeding Intolerance
Official Title
Electrogastrography (EGC) in Premature Infants With Feeding Intolerance: The Effect of Metoclopramide
Study Type
Interventional

2. Study Status

Record Verification Date
December 2003
Overall Recruitment Status
Completed
Study Start Date
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Primary Completion Date
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Study Completion Date
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3. Sponsor/Collaborators

Name of the Sponsor
National Center for Research Resources (NCRR)
Collaborators
Children's Hospital of Philadelphia

4. Oversight

5. Study Description

Brief Summary
Serial EGC measurements in premature infants attempting to correlate EGC measurements with signs of feeding intolerance and response to metoclopramide therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infant, Newborn, Diseases
Keywords
Feeding intolerance, Infant, premature

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Allocation
Non-Randomized

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
metoclopramide

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Minute
Maximum Age & Unit of Time
1 Month
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion: Premature infants. Absence of 1) infection, 2) congenital anomalies, 3) growth retardation
Facility Information:
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

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Electrogastrography (EGC) in Premature Infants With Feeding Intolerance

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