Training Protocol on the Natural History of Tuberculosis

🩺 Protocol Summary

Background: \- Tuberculosis (TB) is an infectious disease that affects numerous people worldwide. Researchers are interested in actively recruiting individuals with TB for research and treatment studies. Objectives: \- To collect blood and other samples to study the natural history of tuberculosis. Eligibility: \- Individuals 2 years of age and older who have either active or latent tuberculosis. Design: * Latent TB patients: Participants will have a single study visit with a physical examination and medical history, and will provide blood samples for testing. * Active TB patients: Participants will have an initial visit with a physical examination and medical history, and will provide blood samples for testing. Participants will also provide sputum samples if required, and may have an optional skin punch biopsy to collect a sample of skin tissue for study. * Treatment for active TB will be provided as part of this protocol. * Active TB participants may be asked to return for study visits every 1-2 months while receiving treatment....

Primary Research Facility: National Institutes of Health Clinical Center (Bethesda, Maryland)

Review these 3 basic logistical and protocol criteria extracted from the public NIH record. (This is a preliminary logistical checklist, not an official clinical eligibility determination).

Diagnosed with, undergoing evaluation for, or seeking treatment related to Mycobacterium Infections?

🔍 Study Population / Focus Area (Source: Protocol Primary Condition)

Aged between 2 Years and 100 Years?

🔍 Protocol Specified Age Range: 2 Years to 100 Years

Able to attend required clinic visits at National Institutes of Health Clinical Center (Bethesda, Maryland)?

🔍 Logistical Requirement: Site at National Institutes of Health Clinical Center

📍 Primary Site Map

Site: National Institutes of Health Clinical Center — Bethesda, Maryland

💰 Clinical Trial Costs & Insurance Coverage

Coverage for clinical trial participation varies depending on your health insurance policy, state legislation, and whether specific procedures are investigational research or routine medical care. Under federal law (Affordable Care Act § 2709), health insurers generally cannot drop coverage or refuse to pay for routine patient care costs incurred in approved clinical trials.

💡 Always ask the study coordinator for the trial's official Informed Consent Form, which outlines all sponsor-funded research items versus procedures billed to your insurance.