Evaluation of Musculoskeletal System Symptoms and Biochemical Parameters in COVID-19
NCT ID: NCT04780555
Last Updated: 2021-08-03
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
150 participants
OBSERVATIONAL
2021-03-01
2021-08-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
COMPARISON OF SYSTEMIC INFLAMMATION-RELATED HEMATOLOGICAL PARAMETERS IN ACUTE AND CHRONIC LOW BACK PAIN
NCT04897620
Musculoskeletal Symptoms in Post Acute Covid-19 Patients
NCT04932889
Muscle Architecture in Ankylosing Spondylitis
NCT06226792
Complete Blood Count-derived Indexes in Inflammatory Modic Changes
NCT06440096
Musculoskeletal Pain in Long COVID
NCT05358119
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Diagnosed with COVID-19
Exclusion Criteria
* Musculoskeletal pains in the previous three months, with diseases capable of causing myalgia prior to diagnosis (such as fibromyalgia and inflammatory muscle disease)
* Cognitive disorders capable of preventing history-taking and physical examination such as mental disability and dementia,
* previous history of headache (migraine, tension type headache)
18 Years
70 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Abant Izzet Baysal University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Elif yaksi
Medical Doctor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Nalan Doğan, MD
Role: PRINCIPAL_INVESTIGATOR
Beykoz State Hospital
Dursun Karakaş, MD
Role: PRINCIPAL_INVESTIGATOR
Sancaktepe Şehit İlhan Varank Research Hospital
Osman Yakşi, MD
Role: PRINCIPAL_INVESTIGATOR
Abant İzzet Baysal University Medical Faculty
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Elif Yakşi
Merkez, Bolu, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AIBU-FTR-EY-02
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.