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Clinical Trials/NCT04780555
NCT04780555
Completed
Not Applicable

Evaluation of Pain Symptoms Correlation With Biochemical and Radiological Findings in COVID-19

Abant Izzet Baysal University1 site in 1 country150 target enrollmentStarted: March 1, 2021Last updated:
ConditionsCovid19

Overview

Phase
Not Applicable
Status
Completed
Enrollment
150
Locations
1
Primary Endpoint
Fibrinogen

Overview

Brief Summary

The neutrophil-lymphocyte ratio (NLR) used to demonstrate inflammatory status in recent years can be calculated by dividing the absolute neutrophil count by the absolute lymphocyte count at routine blood tests.

Detailed Description

Dysregulation in immune responses has been reported in association with hyperinflammation in COVID-19 patients, NLR has been linked to the severity of the patient's clinical status, and an increase in NLR is reported to be an independent risk factor for in-hospital mortality. Pain is a frequently seen symptom at the onset of viral infections and throughout the course of the disease. Although the pain mechanisms triggered by viral pathogens are not yet entirely understood, pain is thought to arise as a result of direct activation of nociceptor neurons by pathogens and their interaction with molecular ligands. Toll-like receptor 7 (TLR7), a pathogen recognition receptor that plays an important role in immune responses to viruses by binding to viral RNA, is known to be involved in pain development in different RNA virus infections. Park et al. showed that extracellular micro RNAs activate nociceptive neurons via the TLR7 pathway. Although these mechanisms have been demonstrated for different viral infections, the viral pathogenesis leading to pain in COVID-19 is still unclear. The purpose of this study was to investigate the prevalence of headache and muscular pain in patients diagnosed with COVID-19 and to determine the relationship between these symptoms and inflammatory parameters.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Aged 18-70
  • Diagnosed with COVID-19

Exclusion Criteria

  • Patients with suspected SARS-CoV-2 infection, with two negative RT-PCR tests, hospitalized in the intensive care unit during inclusion in the study
  • 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)

Outcomes

Primary Outcomes

Fibrinogen

Time Frame: Baseline

Peripheral venous blood specimens were collected using standard surgical procedures

Neutrophil-lymphocyte ratio (NLR)

Time Frame: Baseline

It can be calculated by dividing the absolute neutrophil count by the absolute lymphocyte count at routine blood tests

D-dimer

Time Frame: Baseline

Peripheral venous blood specimens were collected using standard surgical procedures

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Elif yaksi

Medical Doctor

Abant Izzet Baysal University

Study Sites (1)

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