Tuberculosis as a Risk Factor for a Worse Outcome Post-Sars-CoV-2 Infection (Co-TB)

The Aurum Institute NPC

Status: Completed

Conditions: COVID-19; Tuberculosis; Post-acute COVID-19 Syndrome

Study type: Observational

Funder types: Other

Identifiers

NCT05643781

AUR2-8-296

Details and patient eligibility

About

This study has two main objectives. First, the clinical characteristics and outcomes of hospitalized patients with symptomatic Covid-19 disease will be compared between persons with a history of past or current TB infection or disease and those, who have had no TB history. The possible impact of an HIV-coinfection will be also addressed in the planned investigations and analysis. Second, the long-term consequences and clinical outcomes of Covid-19 up to 12 months post-infection will be analysed in both groups (with and without TB history) with the main focus on cardio-pulmonary outcomes.

Full description

This study is retrospective/prospective clinical observational study.

Primary Objective, Study Phase A (hospitalization, retrospective data collection):

• To describe the development and characteristics of Covid-19 pneumonia, clinically and using radiological methods (i.e. CT-thorax)
• To describe disease severity of Covid-19 disease, including treatment in Intensive Care Unit (ICU) and ventilation support measures
• To describe different types of organ failures apart from respiratory failure (e.g. kidney, liver, heart)
• To describe treatment outcomes at discharge, including cause of death
• To assess the significance of additional risk factors such as HIV infection, smoking, malnutrition, etc., for the clinical course and characteristics of a Covid-19 disease Primary Objective, Study Phase B (after end of hospitalization, prospective data collection): The primary objective of the study phase B (after end of hospitalization) is the description of Covid-19 sequelae (focus on cardio-pulmonary morbidity) in patients with and without previous TB disease during a six month follow up period after discharge from hospital, including:
• the description (characteristics and severity) of abnormal function tests and clinical examination results (e.g. in lung function measurement, cardiac tests and ECG, kidney function, neurological & mental tests)
• the definition of time to healing (ad integrum) after a Covid-19 infection
• the studying of chronic restrictions of the long-term quality of life at 12 months after discharge from hospital that are based on chronic organ failures and mental disorders
• the assessment of exacerbations of chronic organ failures, hospitalizations and deaths in 12 months phase after discharge from hospital

Secondary Objective(s):

• To collect longitudinal data that could allow for further insights on whether previous Covid-19 disease results in an increased risk for re-activation of

  /infection with M. tuberculosis

• To perform longitudinal immunological investigations in a sub-set of patients to study Covid-19- immune-activation, depending on M.tb and/or HIVcoinfection status

Enrollment: 157 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Willingness to provide a written informed consent or witnessed oral consent in the case of illiteracy for participation in the study prior to all study-related procedures
• Be ≥ 18 years and <70 years of age
• Having a diagnosis of SARS-CoV-2 infection, confirmed by PCR tests and/or chest CT-scan
• Willing to be tested for active and latent M.tb infection and to provide information on previous TB disease episodes (including agreement for confirmation of active TB disease by the investigators, e.g. via NTP/lab registration number)
• Willing to be tested for HIV, if status is not known or the last documented negative is more than 4 weeks old
• Willingness to comply with the protocol and visit schedule, at the discretion of the investigator
• Having a firm home address that is readily accessible for visiting and is willing to inform the study team of any change of address during study participation

Exclusion criteria

• Has a recent history of a medical condition that is the leading cause for the current clinical symptoms and/or survival, e.g. advanced stages of cancer
• Has severe medical or psychiatric condition which in the opinion of the site investigator or designee, might interfere with the ability to give true informed consent and to adhere to the study requirements.
• Is currently imprisoned
• Confirmed or suspected pregnancy

Trial design

157 participants in 1 patient group

Co-TB Group

Description:

Follow up all participants from hospital discharge until 12 months post-Covid-19 infection. Conduct investigations assessing cardiopulmonary, socioeconomic, quality of life outcomes. No interventions.