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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06328595
Other study ID # Cross sectional
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 22, 2022
Est. completion date August 20, 2023

Study information

Verified date March 2024
Source Syrian Private University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Observation study, shows the relation between musckeloskeletal symptoms with during and post Covid-19 infection, by asking participants questions about there age,job,which vaccination covid participants took, residual area, social status, number of time of covid-19 infection, number of joint affected and duration of joint pain and asking if there any malaise or fatigue


Recruitment information / eligibility

Status Completed
Enrollment 1039
Est. completion date August 20, 2023
Est. primary completion date May 4, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 78 Years
Eligibility Inclusion Criteria: - Participants aged = 18 years with a prior COVID-19 infection or suspicious COVID-19 infection and currently residing in Damascus. Exclusion Criteria: - Participants below 18 years, those unwilling to give consent, individuals with joint surgery history, pregnant women, or those who had taken immunosuppressive drugs before the study.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Syrian Arab Republic Mohamad Zaid Ahmad Abdalla Damascus

Sponsors (1)

Lead Sponsor Collaborator
Syrian Private University

Country where clinical trial is conducted

Syrian Arab Republic, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Demographic characteristics were classified into four groups: Gender, Residual area, education level. Gender was either male or female. Residual area was divided into tow categories: Rural or City. Social status were divided into four types: Single, Married, Divorced, Widow . The study took 6 months to finish it with hard work, it was hard to reach our participants so we didn't only collect our data from google form we also colleted our data from Al-Mouassa University Hospital outpatients clinics and Damascus University
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