Gastroenteritis in Pediatric Population of Qatar (GE)

March 21, 2024 updated by: Hamad Medical Corporation

Epidemiology of Acute Gastroenteritis in the Pediatric Population in Qatar: Causes, Risk Factors, Burden of Disease, Sources and Preventable Measures

Comparison of clinical and laboratory diagnosis for cause of Gastroenteritis(GE) depending on the clinical manifestation.Identifying the sources of viral, bacterial and parasitic GE in Pediatric population of Qatar

Study Overview

Status

Recruiting

Conditions

Detailed Description

Processing of stool samples by molecular method (PCR) for children with GE including complete data collection. Patients are followed up for 14 days

Study Type

Observational

Enrollment (Estimated)

3000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Doha, Qatar, 3050
        • Recruiting
        • Hamad Medical Corporation
        • Contact:
          • Dr.Khalid M Alansari, MD,FRCPC,FAAP(PEM)
          • Phone Number: +97444396006 +97455336166
          • Email: KALANSARI1@hamad.qa

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 14 years (Child)

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

All acute gastroenteritis patients between 3 months to 14 years presenting to PEC centers with acute diarrhea+/- vomiting with or without fever

Description

Inclusion Criteria:

  • All acute gastroenteritis patients between 3 months to 14 years presenting to PEC centers with acute diarrhea+/- vomiting with or without fever

Exclusion Criteria:

  1. Cases of vomiting +/- fever only without diarrhea
  2. Suspicion of surgical abdomen
  3. Bile stained vomitus
  4. Mal-absorption diseases as cystic fibrosis, celiac disease or increased secretion as disaccharides deficiency
  5. Cases of Inflammatory bowel disease
  6. Antibiotic associated diarrhea
  7. Patients with immune deficiency
  8. Patients with chronic diarrhea (>2 weeks of diarrhea)
  9. Patients receiving long term medication for any 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

  • Observational Models: Case-Only
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
sources of viral, bacterial and parasitic GE in the country
Time Frame: 4 years
Prevalence of viral, bacterial and parasitic GE in children < 14 years of age in Qatar will be identified by molecular method sample processing
4 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
seasonal variation of GE in qatar determination
Time Frame: 4 years
seasonal variation of GE in qatar being determined by number of cases reported during each season
4 years
comparing the prevalence of viral GE in vaccinated children in Qatar (against rotavirus) and the other countries which implemented rotavirus vaccine
Time Frame: 4 years
comparing the prevalence of viral GE in vaccinated children in Qatar (against rotavirus) and the other countries which implemented rotavirus vaccine by detection of source of GE in vaccinated children by molecular method.
4 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 Start (Actual)

March 10, 2015

Primary Completion (Estimated)

September 10, 2024

Study Completion (Estimated)

December 10, 2024

Study Registration Dates

First Submitted

January 31, 2017

First Submitted That Met QC Criteria

February 5, 2017

First Posted (Estimated)

February 8, 2017

Study Record Updates

Last Update Posted (Actual)

March 22, 2024

Last Update Submitted That Met QC Criteria

March 21, 2024

Last Verified

February 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 14-00045

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

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