- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03046342
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
Intervention / Treatment
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
- Name: Dr.Khalid Alansari
- Phone Number: +974 55336166
- Email: kalansari1@hamad.qa
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:
- Cases of vomiting +/- fever only without diarrhea
- Suspicion of surgical abdomen
- Bile stained vomitus
- Mal-absorption diseases as cystic fibrosis, celiac disease or increased secretion as disaccharides deficiency
- Cases of Inflammatory bowel disease
- Antibiotic associated diarrhea
- Patients with immune deficiency
- Patients with chronic diarrhea (>2 weeks of diarrhea)
- 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.
Sponsor
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
Additional Relevant MeSH Terms
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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