Monitoring Growth of Preterm Infants

NCT ID: NCT01869153

Last Updated: 2018-09-20

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

TERMINATED

Total Enrollment

48 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-05-31

Study Completion Date

2018-07-10

Brief Summary

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Growth is poor in preterm infants, partly due to difficulty identifying when growth is slow. The investigators will examine the use of a computer program to try and identify periods of growth slowing in preterm babies, and compare those results to the usual assessments made on patient care rounds.

Detailed Description

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We wish to examine the use of a mathematical modeling system to see if it can detect poor growth better (and more quickly) than we can clinically. To do this, we need to know what the clinical team think about a baby's growth day-to-day. However, after rounds the fellow or NNP with fill in a sheet to say what the team thought about the baby's growth (was it okay, too slow, too fast etc.), and whether any changes were made to improve the baby's growth (e.g. increased feed volume, change in composition of feeds etc.). After the baby is discharged home, weight data from the EMR will be entered into the program to try and identify times where growth slowed (or where growth was faster than expected). We will compare the results of the computer program and the record of the clinical teams thoughts on the ward round, to see if the computer program identified growth slowing more quickly than the clinical team did.

Conditions

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Prematurity

Study Design

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Observational Model Type

COHORT

Study Time Perspective

OTHER

Study Groups

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Preterm infants

Preterm infants born at either \<32 weeks gestation or \< 1750g birth weight

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

1. Birth weight \< 1750g gestational age \< 32w at birth

Exclusion Criteria

2. Currently receiving parenteral nutrition or intravenous lipids
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of California, Davis

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ian Griffin, MD

Role: PRINCIPAL_INVESTIGATOR

University of California, Davis

Locations

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NICU, University of California, Davis

Sacramento, California, United States

Site Status

Countries

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United States

Other Identifiers

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UCD-308519

Identifier Type: OTHER

Identifier Source: secondary_id

308519

Identifier Type: -

Identifier Source: org_study_id

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