Clinical Studies2018-10-20T01:16:34+00:00

Clinical Studies

ProLung’s research team is continually expanding clinical evidence for the ProLung Test, bioconductance, and non-invasive lung cancer risk stratification through ongoing clinical studies and trials.

Completed Trials

FML-204

The FML-204 study was a prospective study of 41 patients to evaluate the safety and efficacy of non-invasive, non-radiating bioconductance measurements in distinguishing between malignant and benign lung lesions. No adverse events reported.

FML-204

Transcutaneous Computed Bioconductance Measurement in Lung Cancer
Rex C. Yung, MD; Ming Ying Zeng, MD; Gregory J. Stoddard, MS; Michael Garff, BS; and Karleen Callahan, PhD.
J Thorac Oncol. Vol. 7, No. 4, April 2012

Ongoing Trials

PL-208

This study is intended to evaluate the safety and efficacy of the ProLung Test for risk stratification of patients with pulmonary lesions identified by CT that are suspicious for lung cancer. PL-208 is being conducted at the following research sites:

Huntsman Cancer Institute
Henry Ford Hospital
University of California Los Angeles
Loyola University Health System
Greater Baltimore Medical Center
University of Minnesota Masonic Cancer Center
Medical University of South Carolina
Mayo Clinic

Stanford Health Care
MD Anderson Cancer Center
Intermountain Health Care
University of California San Diego
Providence Healthcare
Wake Forest Baptist Health
Beth Israel Deaconess Boston

CLINICAL TRIALS

If you have been diagnosed with an indeterminate pulmonary nodule, you may eligible to participate in a ProLung clinical trial.
Fill out the form below and we will connect you to the nearest testing location.