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Clinical Trial Summary

The objective of the study is to investigate prevalence of H.Pylori infection among acne vulgaris patients.


Clinical Trial Description

The study included patients with acne vulgaris and healthy control participants. The study recruited both sexes, all grades of acne, adolescents and young adults.

All patients were subjected to complete history, general and skin examination Acne vlugaris Patients were classified into mild, moderate and severe according to the classification of American Academy of dermatology for acne vulgaris.

Detection of H. pylori infection:

Blood and stool samples were taken from each participant and was directly transferred to laboratory for detection of H. Pylori antigen and antibody.

An enzyme-linked immune sorbent assay (ELISA) was used for quantitative assessment of IgG antibodies against H.Pylori in human serum.

A monoclonal antibodies based enzyme-linked immunosorbent assay was used to detect H.Pylori specific antigen in stool samples. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03411733
Study type Observational
Source Sohag University
Contact
Status Completed
Phase
Start date March 1, 2017
Completion date March 1, 2018

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