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Clinical Trials/NCT05835128
NCT05835128
Active, not recruiting
Not Applicable

A Multicentric Prospective Study: Assessment of Pulmonary Long-term Sequelae of Coronavirus Disease 2019 (COVID-19) Pneumonia With Chest Computed Tomography and Pulmonary Function Tests

Centro Hospitalar Universitario do Algarve2 sites in 1 country250 target enrollmentMarch 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COVID-19 Pneumonia
Sponsor
Centro Hospitalar Universitario do Algarve
Enrollment
250
Locations
2
Primary Endpoint
Prevalence of structural lung sequelae after COVID-19 pneumonia
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this prospective multicentric study is to evaluate the presence of long-term pulmonary sequelae in patients who had required hospitalization for treating COVID-19 pneumonia, trough chest CT and pulmonary function tests (PFT).

Secondly we would like to evaluate the possible correlation between the chest CT findings and pulmonary function tests pre-existing co-morbidities and type of therapy used during hospitalization.

Detailed Description

The investigators will invite to participate in this study patients who had been hospitalized with positive test for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) , namely with positive reverse transcription polymerase chain reaction or positive rapid antigen test, and with respiratory insufficiency (at admission or developed during hospital stay), or with viral pneumonia documented with thorax x-ray or Chest CT, during the period between march 2020 and march 2022. Patients who agree to participate and sign the informed consent will be enrolled in the study. Participants will be evaluate in two different periods: approximately 4 to 6 months after hospital discharge and approximately 12 to 14 months after hospital discharge. The first evaluation includes a physical examination at medical post-COVID-19 consultation, pulmonary function tests and reduced dose chest CT. The second evaluation includes a physical examination at medical post-COVID-19 consultation, and will include reduced dose chest CT and pulmonary function tests only if there were significative findings on those exams on the first evaluation, or if there are any clinical significative findings at the present moment. All the evaluations must respect the following time intervals: the pulmonary function tests and the chest CT will be done within a 6 week maximum interval of each other, and both of these examinations will be done within a 8 week maximum interval regarding the clinical evaluation. Demographic and clinical data will be collected by qualified clinical study staff (i.e., by physicians who conduct the post-COVID-19 medical consultation) and the patient will given the EuroQol 5 Dimension 5 Level questionnaire (EQ-5D-3L) to assess the health status. The reduced dose Chest CT will be obtained with the patient in a supine position and with breath-holding following inspiration, in a spiral acquisition mode with a 1 ,5 mm slice thickness and the images will be reviewed by four senior radiologist blinded to clinical and respiratory functional tests results. The pulmonary function tests will be interpreted according to the American Thoracic Society and European Respiratory Society guidelines 2022. The parameters measured included the forced expiratory flow between 25% and 75% of forced vital capacity (FVC), forced expiratory volume (FEV1), FVC/FEV1, vital capacity, total lung capacity, residual volume and the diffusing capacity of lung for carbone monoxide (DLCO), DLCO/Alveolar Volume (AV).

Registry
clinicaltrials.gov
Start Date
March 1, 2020
End Date
December 31, 2024
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Centro Hospitalar Universitario do Algarve
Responsible Party
Principal Investigator
Principal Investigator

Mónica Diniz, MD

Principal Investigator

Centro Hospitalar Universitario do Algarve

Eligibility Criteria

Inclusion Criteria

  • at least 18 years old of age;
  • positive SARS-CoV-2 reverse transcription-polymerase chain reaction on a nasopharyngeal and/or oropharyngeal swab or positive SARS-CoV-2 rapid antigen test
  • hospitalization in one of two hospitals of our institution (university center) in consequence of SARS-CoV-2 related disease between march of 2020 and march of 2022 and having :
  • respiratory insufficiency when admitted or developing after admission or image documented viral pneumonia ;
  • at least one thorax x-ray or lung CT acquired during the hospitalization period

Exclusion Criteria

  • previous lung cancer
  • previous intersticial lung disease

Outcomes

Primary Outcomes

Prevalence of structural lung sequelae after COVID-19 pneumonia

Time Frame: 12 -14 months

evaluate the presence of lung structural sequelae with chest CT

Prevalence of functional lung impairment after COVID-19 pneumonia

Time Frame: 12 -14 months

evaluate the presence of impaired PFT after COVID-19 pneumonia

Association between chest CT findings and PFT impairment after COVID-19 pneumonia

Time Frame: 12-14 months

evaluate the possible correlation between the presence of pulmonary structural alterations on chest CT and the presence of impaired PFT

Secondary Outcomes

  • Association between chest CT findings after COVID-19 pneumonia and pre-existing co-morbidities(12 -14 months)
  • Association between chest CT findings and PFT impairment after COVID-19 pneumonia(4-6 months)
  • Prevalence of structural lung sequelae after COVID-19 pneumonia(4-6 months)
  • Prevalence of functional lung impairment after COVID-19 pneumonia(4-6 months)
  • Association between chest CT findings after COVID-19 pneumonia and therapy used during hospitalization(12-14 months)

Study Sites (2)

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