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Long-term Health Effects of Tuberculosis After Treatment Completion

Follows people who finished tuberculosis treatment to track lung and heart health.

Plain-language title generated from the registry record
Registry title: Post TB Sequelae Study

Key facts

Where
Dhaka, BangladeshSee the site

Where in Bangladesh

  • icddrb Dhaka hospital, Nutrition research divisionDhaka, BangladeshNo longer taking part

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Trial details

Who runs it
International Centre for Diarrhoeal Disease Research, Bangladesh
Trial code
NCT06744179
Record updated
20 December 2024
Original description
The goal of this prospective cohort study is to learn about the long-term health effects of tuberculosis (TB) in children, adolescents, and adults who have completed standard TB treatment in Bangladesh. The study aims to track the evolution of pulmonary and cardiac sequelae within the first two years after TB treatment completion.Read full original descriptionShow less

Understanding the Post-intervention TB Sequelae in Patients After Completion of Standard TB Treatment

The goal of this prospective cohort study is to learn about the long-term health effects of tuberculosis (TB) in children, adolescents, and adults who have completed standard TB treatment in Bangladesh. The study aims to track the evolution of pulmonary and cardiac sequelae within the first two years after TB treatment completion.

The main question it aims to answer is:

Does completing TB treatment result in long-term pulmonary or cardiac health issues (post-TB lung disease, PTLD) in patients compared to those without TB? Additionally, how does this impact children\'s growth, radiological patterns, and overall quality of life?

Participants who have completed anti-TB treatment for the first episode of pulmonary TB and non-TB participants (age- and sex-matched controls) will be followed for two years. The study will take place at multiple sites in Dhaka, including icddr,b Tuberculosis Screening \& Treatment Centers (TBSTC) and Dhaka Shishu Hospital. TB patients and controls will be recruited from Dhaka and surrounding areas.

Over a two-year period, participants will be followed at five key points: within 5-7 days of treatment completion (T0), at 6 months (T1), 12 months (T2), 18 months (T3), and 24 months (T4). Data collection will involve comprehensive clinical evaluations, pulmonary and cardiovascular examinations, laboratory tests, and diagnostic imaging such as chest X-rays, ECGs, and pulmonary function tests.

The study will address several key outcomes, including:

The prevalence and incidence of post-TB lung disease and cardiac sequelae Weight gain and growth in children post-treatment Radiological and ECG patterns post-treatment Mental health and quality of life following TB recovery Associations between demographic, social, and lifestyle factors and post-TB sequelae Through this observational study, researchers hope to contribute valuable insights into the long-term health challenges faced by TB survivors, particularly among children, for whom such data is currently lacking.

Inclusion: Children and adolescents aged 6 months to 15 years; and participants aged \>15 years and above; Successful completion of anti-TB treatment for the first episode of pulmonary TB and or pleural TB, with cure or completion as defined by the NTP; Residing within Dhaka city and be willing to come for follow-up visits.(21); Provide consent for participation to the study; age and sex-matched participants who do not have exposure to TB to compare post-TB sequelae data of study TB patients with that of a local non-TB population.

Exclusion: Tuberculous meningitis, and isolated other extra-pulmonary TB (i.e no concomitant pulmonary TB, or pleural TB), multidrug resistant TB; Past TB disease or anti-TB treatment within last 6 months; Participants getting immunosuppressive therapy or other chemotherapy for malignancy; Pre-existing mental illness. Participants with preexisting mental illness will be identified based on documented prescriptions or medical records provided by a qualified physician; Participants with known congenital heart disease, ischemic heart disease, cystic fibrosis. These participants will be identified based on documented prescriptions or medical records provided by a qualified physician; Past TB disease or anti-TB treatment Any current or past (chronic) respiratory infection or disease; Documented asthma, COPD, heart failure diagnosed by medical personnel; Heavy smoker who consumes more than 20 pieces of cigarettes per day or ≥20 more pack-year; *Patient will be excluded if any two symptoms or signs suggestive of TB is present according to the national guidelines for the management of TB in children and adult; Documented pneumonia, bronchiolitis, bronchitis in last 3 weeks; Documented general wheezing in chest (last 2 years); Self-reported breathing difficulties during mild exercise, or at night. Heavy smoker who consumes more than 20 pieces per day or ≥20 more pack-year.

ClinicalTrials.gov NCT06744179