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CompletedNCT03280784CAOUOEUIAUCHUpdated Nov 10, 2020

Clinical Audit on the Use of Upper Endoscopy in Assist University Children Hospital

An observational study in Upper Gastrointestinal Endoscopy, sponsored by Mahmoud Mohammed Osman Ali. Completed at 1 site in Egypt. Open to participants aged Up to 18 Years. Per ClinicalTrials.gov, last updated 2020-11-10.

Sponsored by Mahmoud Mohammed Osman Ali · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
1
Ages
Up to 18 Years
Sex
All
01

Study summary

this protocol aides to evaluate:( 1)whether upper gastrointestinal endoscopy (UGE) is used appropriately according to the Guideline on pediatric GI endoscopy [1] commissioned by the European Society for Paediatric Gastroenterology Hepatology and Nutrition(ESPGHAN) and the European Society of Gastrointestinal Endoscopy(ESGE). In our hospital setting and(2) whether there is any relationship between appropriateness of gastrointestinal endoscopy and the presence of lesions detected by endoscopy.

Read the detailed description

gastrointestinal endoscopy is a safe and effective procedure. However,complications do exist and procedure-related costs are significant The rapid escalation of the cost of medical care, in the face of limited resources, is making the appropriateness of indications more and more essential to the rational utilization of such resources.Upper Gastrointestinal (UGI) endoscopy in the pediatric population has evolved during the last 30 years with an increasing number of diagnostic and therapeutic applications.

years with an increasing number of diagnostic and therapeutic Technological improvements and endoscopic devices have contributed to the evolution This prospective study is to determine whether upper gastrointestinal endoscopy is used appropriately in our hospital setting according to, the Guideline on pediatric GI endoscopy [1] commissioned by the European Society for Paediatric Gastroenterology Hepatology and Nutrition (ESPGHAN) and the European Society of Gastrointestinal Endoscopy (ESGE). and whether the appropriateness of use Predicts the probability of detecting significant lesions by endoscopy

02

Conditions studied

  • Upper Gastrointestinal Endoscopy
03

Who can participate

Ages eligible
Up to 18 Years
Sexes eligible
All
Sampling method
Non-probability sample

Study population

children admitted at assiut university hospital for upper gastrointestinal endoscopy

Eligibility criteria

Inclusion Criteria:

  • Weight loss,

failure to thrive

Unexplained anemia

Abdominal pain with suspicion of an organic disease

Dysphagia or odynophagia

Caustic ingestion

Recurrent vomiting exclusion criteria

patients with perforated viscous

04

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
1 participant (actual)
Patient registry
No
05

What researchers measure

Primary outcomes

  1. improve the use of upper gastrointestinal endoscopy in assiut university hospital of upper gastrointestinal endoscopy in assiut university children hospital

    appropriateness This prospective study is to determine whether upper gastrointestinal endoscopy is used appropriately in our hospital setting according to, the Guideline on pediatric GI endoscopy \[1\] commissioned by the European Society for Paediatric Gastroenterology Hepatology and Nutrition (ESPGHAN) and the European Society of Gastrointestinal Endoscopy (ESGE). and whether the appropriateness of use Predicts the probability of detecting significant lesions by endoscopy

    Time frame: One year

06

Study locations

1 site
  • Assiut university children hospital
    Assiut, Egypt
07

Registry details

Key details

Study ID
NCT03280784
Lead sponsor
Mahmoud Mohammed Osman Ali
Collaborators
Assiut University
Responsible party
Mahmoud Mohammed Osman Ali (principle investigator, Assiut University) — Sponsor-investigator
First posted
Sep 13, 2017
Start date
Sep 20, 2017
Primary completion
Sep 20, 2018
Completion
Apr 30, 2020
Last update
Nov 10, 2020

Study contacts

mahmoud mohammed, MD
principal investigator · Assiut

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2020. You cannot join it, but the record below documents what was studied.

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