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Recruiting NCT06706596

A Systemic Screening for TB Disease in High-risk Groups in Barcelona

Observational Tuberculosis Tuberculosis, Pulmonary

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Screening for TB symptoms, Chest X-ray.
Who it may be relevant to
Registry conditions: Tuberculosis, Tuberculosis, Pulmonary. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Spain
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Implementing a Systemic Screening for TB Disease in High-risk Groups in Barcelona Area

Overview

The purpose of this screening study is to identify and screen vulnerable population in Barcelona for active pulmonary tuberculosis

Detailed description

If eligible and verbal consent is obtained, individuals:

1. Will attend a small talk/lecture about Tuberculosis (TB) disease 2. Will be interviewed and screened for the presence of TB symptoms: cough, blood in sputum, fever, weight loss, night sweats and chills lasting for \>2 weeks 3. Individuals screened positive for TB will be referred to the hospital for further testing (Chest X-ray, visit, lab tests)

Interventions

  • Other Screening for TB symptoms
    Individuals will be screened for cough, blood in sputum, fever, weight loss, night sweats and chills lasting for \>2 weeks
  • Diagnostic test Chest X-ray
    Chest X-ray will be performed to diagnose or exclude TB

Primary outcome measures

  • Number of individuals who screen positive for pulmonary TB symptoms [Time frame: 1 day]
  • Number of individuals who are diagnosed with pulmonary TB symptoms [Time frame: 1 month]
Secondary outcome measures (2)
  • Cost-effectiveness analysis [Time frame: 1 day]
  • Time spent during screening [Time frame: 1 day]

Eligibility criteria

Inclusion criteria

-Belonging to a population at high risk for tuberculosis (TB)

Exclusion criteria

-Not belonging to a population at high risk for tuberculosis (TB)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

Spain · 1 center
  • IGTP — Badalona

Identifiers

NCT: NCT06706596 · SYS-TB-S

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗