- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00248391
The Influence of Feeding Position on Pulmonary Morbidity in Young Children
October 25, 2007 updated by: Hadassah Medical Organization
Supine feeding position is associated with serous otitis media.
The hypothesis is that supine feeding is associated with recurrent otitis media, tonsillar and adenoid hypertrophy and recurrent pneumonia secondary to recurrent aspiration.
Study Overview
Status
Unknown
Intervention / Treatment
Detailed Description
The aim of the study is to compare two "mother and child health clinic" stations with similar socioeconomic background.
Mothers from the study station will be instructed to feed their children only in an upright position since birth.
In the control station mothers will continue to feed their children as usual.
Pulmonary morbidity will be evaluated prospectively through the computer system of the insurance companies.
Study Type
Interventional
Enrollment (Anticipated)
2000
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Jerusalem, Israel, P.P.Box 12000
- Hadassah Medical Organization, Jerusalem, Israel
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
3 months to 1 year (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Newborn
- Mother's compliance
Exclusion Criteria:
- Bronchopulmonary dysplasia (BPD)
- Asthma
- Cystic fibrosis
- Heart disease
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Allocation: Non-Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
pulmonary and ear-throat-nose morbidity
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|
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medical costs
Time Frame: measured every 3 months
|
measured every 3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Avraham Avital, Prof, Hadassah Medical Organization
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Completion (Anticipated)
January 1, 2008
Study Registration Dates
First Submitted
November 3, 2005
First Submitted That Met QC Criteria
November 3, 2005
First Posted (Estimate)
November 4, 2005
Study Record Updates
Last Update Posted (Estimate)
October 26, 2007
Last Update Submitted That Met QC Criteria
October 25, 2007
Last Verified
October 1, 2006
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- avitalbotlitis- HMO-CTIL
- no grant meanwhile
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.