Pulmonary Tuberculosis Sequelae in Patients With COPD

Study Results

Results pending

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.

Recruitment Status

UNKNOWN

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-05-01

Study Completion Date

2021-05-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

It is known that there is a complex relationship between tuberculosis and COPD. Post-tuberculosis airway disease or COPD associated with tuberculosis occurs in a significant portion of tuberculosis patients. However, it was observed that mortality rates and exacerbation rates of COPD patients with tuberculosis sequel were higher. However, the effect of tuberculosis sequela on functional outcomes in COPD patients has not been investigated in the studies.

The aim of this study is to determine whether the previous tuberculosis sequelae has a functional effect on patients with COPD.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

The Role of Tuberculosis in Chronic Obstructive Lung Disease

NCT02759848

The Role of Tuberculosis in COPD

COMPLETED

Clinical Features of Smoker Patients With Chronic Obstructive Pulmonary Disease

NCT04711629

Copd Smoking

UNKNOWN NA

The Clinical Characteristics, Treatment and Prognosis of Tuberculosis-associated COPD

NCT06074042

COPD

RECRUITING

Are Comorbidities Related to Frequent Severe Exacerbations of AECOPD

NCT05504993

Chronic Obstructive Lung Disease Acute Exacerbation of COPD Comorbidities and Coexisting Conditions

COMPLETED

Research of Burden of Interstititial Lung Diseases in Turkey

NCT03995654

Lung Diseases, Interstitial Fibrosis Lung

UNKNOWN

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

This research is planned as a cross-sectional study. It will start within one week following the approval of the ethics committee and will be completed within one year. The universe of the study is S.B.Ü. Dr. Suat Seren Chest Diseases and Surgery Training and Research Hospital consists of patients who apply to Pulmonary Rehabilitation Outpatient Clinic. Participants will consist of two different groups: COPD patients with tuberculosis and COPD patients without tuberculosis. The voluntary principle will be taken into account in participating in the research.

Within the scope of the evaluation; Demographic and clinical information of the people who will participate in the study will be recorded, and Thorax CT and PFT examinations performed within the polyclinic service within the last 1 month will be evaluated. Saint George Respiratory Questionaire (SGRQ), 6-minute walk test (6MWT), Medical Research Council Dyspnea Scale (MRC), COPD assessment test (CAT) will be applied to the patients. Regarding the illness histories, the number of hospitalizations and emergency admissions in the last 1 year will be recorded. Detailed tuberculosis anamneses will also be taken from patients with tuberculosis sequelae.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Copd Tuberculosis Quality of Life

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

COPD patients with tuberculous sequelae

Functional Outcome Measurements

Intervention Type OTHER

Dyspnea Exercise capacity Quality of life assessment

COPD patients without tuberculosis sequela

COPD patients with tuberculous sequelae

Functional Outcome Measurements

Intervention Type OTHER

Dyspnea Exercise capacity Quality of life assessment

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Functional Outcome Measurements

Dyspnea Exercise capacity Quality of life assessment

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Volunteering to participate in the study
* Being over 18 years old
* Having thorax CT in the last 1 month
* Having PFT examination performed in the last 1 month