Skip to main content
Clinical Trials/NCT06328595
NCT06328595CompletedNot Applicable

A Cross-Sectional Analysis of Muscular and Joint Symptoms in COVID-19 Patients: Insights From Syria

Syrian Private University1 site in 1 country1,039 target enrollmentStarted: April 22, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
1,039
Locations
1
Primary Endpoint
The Demographic characteristics were classified into four groups: Gender, Residual area, education level.

Study Overview

Brief 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

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
18 Years to 78 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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.

Outcomes

Primary Outcomes

The Demographic characteristics were classified into four groups: Gender, Residual area, education level.

Time Frame: 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

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 .

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Syrian Private University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mohamad Zaid Mohamad Samer Ahmad Abdalla

Dr in Damascus university in general internal medicine

Syrian Private University

Study Sites (1)

Loading locations...

Similar Trials