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NCT04433754 Clinical Trial

The Development of Pancreatic Injury in the Course of Severe Acute Respiratory Syndrome Coronavirus 2 Infection

Pancreatitis Clinical Trial

Official title:
Pancreatic Injury in Patients With COVID-19 Disease

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04433754
Other study ID # UsakU-Cevdet2
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2020
Est. completion date June 12, 2020

Study information
Verified date June 2020
Source Usak University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Although COVID-19 disease due to Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) affects the respiratory tract, heart and coagulation system, symptoms of gastrointestinal system involvement such as abdominal pain, nausea, vomiting and diarrhea are also common.

In this study, it was aimed retrospective analysis of clinical and laboratory data of patients who developed pancreatic injury in the course of COVID 19 disease.

Recruitment information / eligibility
Status Completed
Enrollment 500
Est. completion date June 12, 2020
Est. primary completion date June 11, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with amylase and lipase levels measured during covid-19 disease with or without pneumonia

Exclusion Criteria:

- Patients with pregnancy

- Patients whose amylase and lipase levels were not measured during covid 19 disease

- Patients with known solid organ malignacy

- Patients with known hematologic malignacy

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• biochemical analysis
cRP, d-dimer levels and lymphocyte counts will be compared

Locations
Country Name City State
Turkey Usak University Training and Research Hospital Usak

Sponsors (1)
Lead Sponsor Collaborator
Usak University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary to compare presence of fever in patients with and without pancreatic injury To evaluate the frequency of presence of fever in patients with and without pancreatic injury 3 month
Primary to compare presence of dyspnea in patients with and without pancreatic injury To evaluate the frequency of presence of dyspnea in patients with and without pancreatic injury 3 month
Primary To compare cRP levels in patients with and without pancreatic injury CRP levels will be compared in patients with and without pancreatic injury 3 month
Primary To compare d-dimer levels in patients with and without pancreatic injury D-Dimer levels will be compared in patients with and without pancreatic injury 3 month
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