Impact of Blood Volume on QuantiFERON Test Accuracy

Overview

About this study

The purpose of this study is to evaluate whether the volume of whole blood collected in QuantiFERON testing tubes impacts the accuracy of test results. 

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • 18 years of age or older.
  • Diagnosis of latent tuberculosis infection (LTBI).

Exclusion Criteria: 

  • Inability to sign informed consent.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 12/22/23. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Patricio Escalante, M.D., M.S.

Closed for enrollment

Contact information:

Kale Daniel

(507) 266-4541

Daniel.Kale@mayo.edu

More information

Publications

Publications are currently not available