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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04803162
Other study ID # STM.C130.17.045
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date November 14, 2017
Est. completion date December 2021

Study information

Verified date March 2021
Source Wroclaw Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the project is to assess the correlation between the results of high-resolution oesophageal manometry and specific biomarkers of inflammation (eotaxin 3, major basic protein, IL-5, IL-13, TGF-beta1) with symptoms of dysphagia, endoscopic and histological features and the assessment of quality of life in patients with eosinophilic esophagitis. Research hypothesis: The results of high resolution esophageal manometry (HRM) and specific inflammatory biomarkers correlate with symptoms of dysphagia, endoscopic and histological features, and assessment of quality of life in patients with eosinophilic oesophagitis. HRM, along with the determination of specific inflammatory biomarkers present in the peripheral blood, may serve as a less invasive method of assessing the effectiveness of the treatment of eosinophilic oesophagitis in relation to the currently used endoscopic examinations.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 58
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients over 18 years of age, - patients referred for endoscopic diagnostics due to dysphagia. Exclusion Criteria: - already diagnosed chronic diseases with possible eosinophilic infiltration of the gastrointestinal tract (eosinophilic esophagitis, eosinophilic gastroenteritis, Crohn's disease, celiac disease), - rheumatological, dermatological and genetic disorders with possible peripheral eosinophilia, - dysphagia caused by a diagnosed neoplastic infiltration of the esophagus.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
High-resolution manometry
The parameters of high-resolution esophageal manometry will be compared between EoE patients and controls.
Serum biomarkers
The serum levels of IL-5, IL-13, TGF-ß1, MBP and eotaxin 3 will be compared between EoE patients and controls.
Gastrointestinal Quality of Life index
The Gastrointestinal Quality of Life index (GIQLI) will be compared between EoE patients and controls.
Drug:
Omeprazole 20 MG Oral Tablet
The parameters of high-resolution esophageal manometry and serum levels of IL-5, IL-13, TGF-ß1, MBP and eotaxin 3 will be compared in the group of patients with EoE at enrollment in the project and after 3 months of treatment with PPIs.

Locations

Country Name City State
Poland Department of Gastroenterology and Hepatology, Wroclaw Medical University Wroclaw Borowska 213

Sponsors (1)

Lead Sponsor Collaborator
Wroclaw Medical University

Country where clinical trial is conducted

Poland, 

Outcome

Type Measure Description Time frame Safety issue
Primary High-resolution manometry The parameters of high-resolution esophageal manometry will be compared between EoE patients and controls. 3 months
Primary Serum biomarkers The serum levels of IL-5, IL-13, TGF-ß1, MBP and eotaxin 3 will be compared between EoE patients and controls. 3 months
Primary Gastrointestinal Quality of Life index The Gastrointestinal Quality of Life index (GIQLI) will be compared between EoE patients and controls. 3 months
Secondary High-resolution manometry in the group of patients with EoE The parameters of high-resolution esophageal manometry will be compared in the group of patients with EoE at enrollment in the project and after 3 months of treatment with PPIs. 3 months
Secondary Serum biomarkers in the group of patients with EoE The serum levels of IL-5, IL-13, TGF-ß1, MBP and eotaxin 3 will be compared in the group of patients with EoE at enrollment in the project and after 3 months of treatment with PPIs. 3 months
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