Actively Recruiting

All Genders
Healthy Volunteers
ID06706596

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

Led by Fundació Institut Germans Trias i Pujol · Updated on 2024-11-29

3000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

F

Fundació Institut Germans Trias i Pujol

Lead Sponsor

C

Catalan Public Health Agency

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a screening study to identify people at high risk of active pulmonary tuberculosis (TB) in the Barcelona area. The study focuses on vulnerable groups such as war refugees, migrants, and individuals living in socio-economically deprived neighborhoods. The goal is to detect TB symptoms early and refer those who screen positive for further medical evaluation. Participants who qualify and provide verbal consent will first attend an educational talk about TB. They will then be interviewed and screened for symptoms like cough, blood in sputum, fever, weight loss, night sweats, and chills lasting more than two weeks. Those who show symptoms will be referred to a hospital for additional examinations, including chest X-rays and laboratory tests. During the study, researchers will track how many individuals screen positive for TB symptoms and how many are ultimately diagnosed. They will also analyze the cost-effectiveness and time spent during the screening process. The study aims to improve early detection and management of TB in high-risk populations through this observational approach.

CONDITIONS

Brief Title

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

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Belonging to a population at high risk for tuberculosis (TB)
Not Eligible

You will not qualify if you...

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

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 1 month

Participants who screen positive for TB symptoms undergo diagnostic testing including a chest X-ray and laboratory tests to confirm the presence of tuberculosis.

1 to 2 visits depending on diagnostic procedures

Long-term Monitoring

Duration - Not specified

Participants diagnosed with TB may be monitored over time as part of observational follow-up.

Additional visits as needed

Trial Site Locations

Total: 1 location

1

IGTP

Badalona, Spain, 08916

Actively Recruiting

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Research Team

C

Cristina Vilaplana, MD, PhD

N

Nino Gogichadze, MD, MsC

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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