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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04490772
Other study ID # COVID gastro intestinal
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date July 2020
Est. completion date September 2020

Study information

Verified date July 2020
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Patients confirmed COVID-19 with gastrointestinal manifestations will be included. Characteristics and outcomes will be described for them.


Description:

Patients diagnosed as confirmed Covid-19 according to WHO and Egyptian Ministry of Health and Population (MOH) definitions will be included.The following will be done for all patients:

Demographic characters; age, sex, presence of co-morbidities such as hypretension, diabetes mellitus, obstructive lung diseases, ischemic heart diseases...etc, history of contact to covid-19 patients or recent travelling abroad.Clinical Characteristics: By recording of clinical manifestation such as fever, cough, shortness of breath, sore throat, change in taste or smell, nausea,vomiting and diarrhea will be done. Complications and the type of treatment received by the patients will also be described including mechanical ventilation.

Laboratory data will also be included : blood picture, liver enzymes, ESR,CRP, serum ferritin, D-dimer and troponin.

Follow up of the patients will be done until improvement, deaths or complications to determine disease outcomes.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date September 2020
Est. primary completion date September 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Confirmed Covid-19 with GIT manifestations

Exclusion Criteria:

- Patients refuse to participate

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Laboratory tests
Laboratory tests such as CBC, Liver function and CRP

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical data questionnaire Clinical characteristics of age, sex, comorbidities and symptoms. 2 months
Primary Tests such as CBC Laboratory characters 2 months
Primary liver function test Laboratory characters 2 months
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