CClinicalTrials.gg
Status unknownNCT00484952Updated Aug 1, 2007

Surveillance of Hospitalizations Due to Rotavirus Infections Among Children From Israel

An observational study in Rotavirus Infections, sponsored by Hillel Yaffe Medical Center. Status unknown at 2 sites in Israel. Open to participants aged 1 Month to 5 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2007-08-01.

Sponsored by Hillel Yaffe Medical Center · Observational

The sponsor has not verified this record recently (last verified Jun 2007), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Defined population
Time perspective
Prospective
Enrollment
2,500
Ages
1 Month to 5 Years
Sex
All
01

Study summary

Objectives

  1. To determine the burden and characteristics of rotavirus-associated hospitalizations among children under five years of age of northern Israel
  2. To identify potential risk factors of rotavirus infections associated with hospitalizations among Jewish and Arab children younger than five years of age.

Methods:

Study design: A two-year prospective study and a nested case control study will be carried out Collection of data: Questionnaires will be filled in with demographic characteristics of patients and data on the clinical manifestation of the diarrheal episode leading to hospitalization. Stool specimens will be systematically collected from all children hospitalized because of diarrheal diseases and examined for rotavirus and for bacterial and protozoan enteropathogens. Positive samples for rotavirus will be tested for G and P genotypes.

For the nested case control study additional data will be obtained from parents' interviews on variables such as: parents' education, parents' age, parents' occupation, no. of siblings, age of siblings, breastfeeding etc. to identify potential risk factors for rotavirus diarrhea necessitating hospitalization.

Data analysis: Methods of descriptive statistics / epidemiology will be applied to determine the characteristics of the burden of rotavirus-associated hospitalizations (the distribution of diarrhea associated hospitalizations by etiology, rates of rotavirus diarrheal diseases in Jewish and Arab children, age specific rates of rotavirus infections, the percentage of hospitalizations due to rotavirus diarrhea by month, etc.

For the nested case control study, univariate analysis will be first performed using Student t test for continuous variables and chi square test for categorical variables to study the statistical significance of predictive factors of rotavirus diarrheal diseases necessitating hospitalization. Multivariate analysis using logistic regression models will be performed to study the independent effect of each variable. Odds ratios (OR) and 95% CI will be computed for each variable. Two tailed p \< 0.05 will be considered significant.

Read the detailed description

Rationale: Vaccination against rotavirus is the most appropriate mean for prevention and control of rotavirus infections. Israel is highly endemic for diarrheal diseases but limited data exist on the burden \& epidemiology of rotavirus diarrheal diseases. Such data are essential to assess the relevance of potential future vaccination against rotavirus-associated gastroenteritis in Israel.

Objectives

  1. To determine the burden and characteristics of rotavirus-associated hospitalizations among children under five years of age of northern Israel
  2. To identify potential risk factors of rotavirus infections associated with hospitalizations among Jewish and Arab children younger than five years of age.

Methods:

Study design: A two-year prospective study and a nested case control study will be carried out Study population: About 45000 children aged less than five years, residing in the catchment areas of three pediatric wards of sentinel hospitals (Laniado - Netanya, Carmel - Haifa \& Hillel Yaffe -Hadera) will be under daily surveillance for hospitalizations due to rotavirus diarrheal diseases for two years. The catchment area of the 3 hospitals has a good representation of both Jewish and Arab pediatric population. During the study period we expect 400 hospitalizations due to diarrheal diseases and 80 hospitalizations due to rotavirus gastroenteritis annually, in each of the three hospitals (i.e. 480 cases of rotavirus- diarrheal disease in the two year study). 100 subjects hospitalized because of rotavirus associated diarrhea and 100 controls matched by age, gender and origin will be recruited for the nested case-control study.

Collection of data: Questionnaires will be filled in with demographic characteristics of patients and data on the clinical manifestation of the diarrheal episode leading to hospitalization. Stool specimens will be systematically collected from all children hospitalized because of diarrheal diseases and examined for rotavirus and for bacterial and protozoan enteropathogens. Positive samples for rotavirus will be tested for G and P genotypes.

For the nested case control study additional data will be obtained from parents' interviews on variables such as: parents' education, parents' age, parents' occupation, no. of siblings, age of siblings, breastfeeding etc. to identify potential risk factors for rotavirus diarrhea necessitating hospitalization.

Data analysis: Methods of descriptive statistics / epidemiology will be applied to determine the characteristics of the burden of rotavirus-associated hospitalizations (the distribution of diarrhea associated hospitalizations by etiology, rates of rotavirus diarrheal diseases in Jewish and Arab children, age specific rates of rotavirus infections, the percentage of hospitalizations due to rotavirus diarrhea by month, etc.

For the nested case control study, univariate analysis will be first performed using Student t test for continuous variables and chi square test for categorical variables to study the statistical significance of predictive factors of rotavirus diarrheal diseases necessitating hospitalization. Multivariate analysis using logistic regression models will be performed to study the independent effect of each variable. Odds ratios (OR) and 95% CI will be computed for each variable. Two tailed p \< 0.05 will be considered significant.

02

Conditions studied

  • Rotavirus Infections

Keywords

  • rotavirus
  • diarrheal diseases
  • hospitalizations
  • multicenter
  • children
  • under five year old
  • Hospitalization due to diarhheal diseases
  • Hospitalization due to rotavirus gastroenteritis
  • Nosocomial rotavirus infections
03

In context

Infections

6,687 studies on the registry are indexed under Infections; 807 are open to participants now.

This study's planned enrollment of 2,500 is above the median of 240 across 2,136 observational studies indexed under Infections.

Browse Infections studies →

Lead sponsor

Hillel Yaffe Medical Center is the lead sponsor of 301 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Month to 5 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Age: under five year old
  • Hospitalization due diarrheal disease within the study period in the pediatric wards participating in the study
  • Controls: hospitalization due non-gastrointestinal causes within the study period in the pediatric wards participating in the study

Exclusion criteria

Exclusion Criteria:

  • Refusal
05

Study design

Observational model
Defined population
Time perspective
Prospective
Enrollment
2,500 participants (estimated)
06

Study locations

2 sites
  • Carmenl Medical Center
    Haifa, Israel
    • Moshe Efrat, MD · Contact
    • Moshe Efrat, MD · Principal investigator
  • Laniado Medical Center
    Netanya, Israel
    • Uri Robenstien, MD · Contact
    • Uri Robenstein, MD · Principal investigator
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 1, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00484952
Lead sponsor
Hillel Yaffe Medical Center
Collaborators
Tel Aviv University, Laniado Hospital, Carmel Medical Center, The Meshulash Research and Development Center Kfar Qaraa, Ministry of Health, Israel
First posted
Jun 12, 2007
Start date
Sep 2007
Completion
Sep 2009 (estimated)
Last update
Aug 1, 2007

Study contacts

Eias Kasem, MD
Contact
eiaska@hy.health.gov.il
+972-4-6304331
Dani Cohen, MPH, PhD
Contact
dancohen@post.tau.ac.il
+972-3-640-7591
Dani Cohen, PhD
principal investigator · Tel Aviv University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2007. You cannot join it, but the record below documents what was studied.

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