Diagnostic Yeild of Esophagogastrodudenoscopy in Pediatric Chronic Abdominal Pain
NCT ID: NCT07154940
Last Updated: 2025-09-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
100 participants
OBSERVATIONAL
2025-10-31
2027-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Alarm symptoms (e.g., weight loss, anemia, Hematemesis, Dysphagia, persistent vomiting, nocturnal pain)
* Failure of empiric therapy (e.g., proton pump inhibitors or dietary modifications)
* Suspicion of an underlying organic disease (e.g., celiac disease or Helicobacter pylori infection)
Exclusion Criteria
2. Children aged less than 6 years and more than 18 years
3. Recent use of proton pump inhibitors (within 2 weeks) or antibiotics (within 4 weeks) before endoscopy.
4. Children meeting the criteria of functional abdominal pain according to Rome IV criteria in which was defined as as recurrent or chronic abdominal pain that is not explained by another medical condition and is not solely associated with physiological events like eating or menstruation. It must occur at least 4 times per month for at least 2 months, and diagnostic evaluation should rule out other conditions .
5. Children with contraindications to undergoing EGD (e.g., severe respiratory or cardiac conditions).
6. Children who refuse to participate or whose parents do not provide consent.
7. Children previously diagnosed with recurrent abdominal pain -
6 Years
18 Years
ALL
No
Sponsors
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Assiut University
OTHER
Responsible Party
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Amal Ayoub Ibrahim Hinnawi
Resident doctor
Other Identifiers
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AUCH AssiutU
Identifier Type: -
Identifier Source: org_study_id
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