Trial record 2 of 12 for:    Open Studies | "Palatine Tonsil"

The Influence of Feeding Position on Pulmonary Morbidity in Young Children

The recruitment status of this study is unknown because the information has not been verified recently.
Verified October 2006 by Hadassah Medical Organization.
Recruitment status was  Not yet recruiting
Sponsor:
Information provided by:
Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT00248391
First received: November 3, 2005
Last updated: October 25, 2007
Last verified: October 2006
  Purpose

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.


Condition Intervention
Pulmonary Diseases
Tonsillar Hypertrophy
Otitis Media
Dental Caries
Behavioral: upright feeding

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Factorial Assignment
Masking: Open Label
Official Title: The Influence of Feeding Position on Pulmonary Morbidity in Young Children

Resource links provided by NLM:


Further study details as provided by Hadassah Medical Organization:

Primary Outcome Measures:
  • pulmonary and ear-throat-nose morbidity
  • medical costs [ Time Frame: measured every 3 months ]

Estimated Enrollment: 2000
Estimated Study Completion Date: January 2008
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.

  Eligibility

Ages Eligible for Study:   3 Months to 12 Months
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Newborn
  • Mother's compliance

Exclusion Criteria:

  • Bronchopulmonary dysplasia (BPD)
  • Asthma
  • Cystic fibrosis
  • Heart disease
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00248391

Contacts
Contact: Avraham Avital, Prof 972-2-6777782 avital@hadassah.org.il

Locations
Israel
Hadassah Medical Organization, Jerusalem, Israel Not yet recruiting
Jerusalem, Israel, P.P.Box 12000
Contact: Avraham Avital, Prof    972-2-6777782    avital@hadassah.org.il   
Sponsors and Collaborators
Hadassah Medical Organization
Investigators
Principal Investigator: Avraham Avital, Prof Hadassah Medical Organization
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00248391     History of Changes
Other Study ID Numbers: avitalbotlitis- HMO-CTIL, no grant meanwhile
Study First Received: November 3, 2005
Last Updated: October 25, 2007
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Keywords provided by Hadassah Medical Organization:
adenoid hypertrophy
feeding position
supine
upright
pneumonia
wheezing
otitis
adenoid
tonsil
caries

Additional relevant MeSH terms:
Dental Caries
Hypertrophy
Lung Diseases
Otitis
Otitis Media
Tooth Demineralization
Tooth Diseases
Stomatognathic Diseases
Pathological Conditions, Anatomical
Respiratory Tract Diseases
Ear Diseases
Otorhinolaryngologic Diseases

ClinicalTrials.gov processed this record on August 28, 2014