Persistence of Symptoms After Improvement of Acute COVID-19
NCT ID: NCT04764773
Last Updated: 2021-11-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
172 participants
OBSERVATIONAL
2020-05-01
2021-03-31
Brief Summary
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Detailed Description
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Patients with severe complex illness, pregnant or lactating females and patient who refuse to participate or give complete detailed history will be excluded from the study.
The study protocol will be approved by the scientific Research Ethical committee, Faculty of Medicine, Sohag University A control group of healthy volunteer who were age and sex matched to our patient were included
After taken informed consent according to Sohag University Ethical Committee, the baseline data will be collected from Sohag isolation hospital of COVID19, then the researchers will perform interviews with all participants through mobile phone. The interview will include:
* Name (Optional)
* Age
* Sex
* Occupation
* Presence of DM, HTN or any chronic illness
* Asking about Smoking
* The date of catching COVID19 infection
* Asking about symptoms of COVID19 infection and duration of each symptom.
* Asking about any residual symptoms as: Fatigue, Myalgia, Arthralgia, Chest pain, Dyspnea, Dry cough, Productive cough, Sore Throat, Anosmia, Loss of taste sensation, Nausea, Anorexia, Diarrhea, Redness of the eye, Headache, Confusion and Depression
Statistical analysis:
Data will be analyzed using STATA version 14.2 (Statistical Software: Release 14.2 College Station, TX: Stata Corp LP). Quantitative data will be represented as mean, standard deviation, median and range. normally distributed. Qualitative data will be presented as numbers and percentages. Chi square test will be used for comparison of percentages in different groups. P value will be considered significant if it was less than 0.05.
Conditions
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Keywords
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Case
Patient who had COVID19 infection
No intervention
No intervention
control
healthy volunteer who were age and sex matched with our patients
No intervention
No intervention
Interventions
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No intervention
No intervention
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
ALL
Yes
Sponsors
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Sohag University
OTHER
Responsible Party
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Mona Mohammed Abdelrhman
Principal investigator
Principal Investigators
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Noha Abdelrahman, assistant-lecturer
Role: STUDY_CHAIR
Sohag University
Locations
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Mona Mohammed Abdelrahman
Sohag, , Egypt
Countries
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References
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Xiong Q, Xu M, Li J, Liu Y, Zhang J, Xu Y, Dong W. Clinical sequelae of COVID-19 survivors in Wuhan, China: a single-centre longitudinal study. Clin Microbiol Infect. 2021 Jan;27(1):89-95. doi: 10.1016/j.cmi.2020.09.023. Epub 2020 Sep 23.
Abdelrahman MM, Abd-Elrahman NM, Bakheet TM. Persistence of symptoms after improvement of acute COVID19 infection, a longitudinal study. J Med Virol. 2021 Oct;93(10):5942-5946. doi: 10.1002/jmv.27156. Epub 2021 Jul 2.
Other Identifiers
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Soh-Med-21-02-46
Identifier Type: -
Identifier Source: org_study_id