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Electrogastrography (EGC) in Premature Infants With Feeding Intolerance

NCT ID: NCT00008736

Last Updated: 2005-06-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Study Classification

INTERVENTIONAL

Brief Summary

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

Detailed Description

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Conditions

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Infant, Newborn, Diseases

Keywords

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Feeding intolerance Infant, premature

Study Design

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Allocation Method

NON_RANDOMIZED

Primary Study Purpose

TREATMENT

Interventions

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metoclopramide

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

Premature infants. Absence of 1) infection, 2) congenital anomalies, 3) growth retardation
Minimum Eligible Age

1 Minute

Maximum Eligible Age

1 Month

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Children's Hospital of Philadelphia

OTHER

Sponsor Role collaborator

National Center for Research Resources (NCRR)

NIH

Sponsor Role lead

Locations

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Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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NCRR-M01RR00240-1724

Identifier Type: -

Identifier Source: org_study_id