- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04941053
Seroprevalence of COVID-19 (cov prevalence)
Seroprevalence of COVID19 in Sohag Governorate Egypt
Study Overview
Detailed Description
Aims of work:
A cross-sectional study to detect the seroprevalence to COVID 19 in chronic hemodialysis patients and compare it with the COVID 19 seroprevalence in healthy control in Sohag governorate Egypt
Methods:
After taken informed consent according to Sohag University Ethical Committee A questionnaire on coronavirus symptoms will be asked including epidemiological characters and history of previous COVID 19 infection and infection control measures to prevent it
5 ml of the blood sample will be taken for IgG antibodies testing with a chemiluminescent microparticle immunoassay.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Sohag, Egypt, 82733
- Sohag University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- patient accept to participate
Exclusion Criteria:
- vaccinated people
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
group 1 chronic haemodialysis patients
seroprevalnce of COVID 19
|
seroprevalnce
|
healthy control
seroprevalnce of COVID 19
|
seroprevalnce
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
seroprevalnce
Time Frame: 3-6-2021 to 30-8-2021
|
antibody measurement
|
3-6-2021 to 30-8-2021
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: N S shafik, lecturer, Sohag University Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Soh-Med-21-04-33
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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