Using E-Nose Technology to Measure Response to Treatment in People With Malignant Pleural Mesothelioma

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30-85
SponsorMemorial Sloan Kettering Cancer Center

About this trial

The researchers are doing this study to test the ability of a new technology called breathprinting, or electronic nose (E-Nose), to measure how people respond to standard treatment for malignant pleural mesothelioma (MPM). The researchers will study how E-Nose breathprints change over time as people receive standard treatment for MPM. They will also look at how changes in people's E-Nose breathprints compare to changes in their standard imaging scans and in biomarkers of MPM in their blood.

Eligibility criteria

Qualifiers

Aged 30-85 years

No history of thoracic cancer or extrathoracic cancer potentially involving pleural metastases (i.e., breast, gastric, colon, or pancreas cancer)

Recent diagnosis of MPM

Documented, signed, and dated informed consent, obtained before any procedures, for the proposed research study, and signed standard surgical consent for surgical resection

Disqualifiers

Aged <30 or >85 years at the first outpatient visit

History of thoracic or extrathoracic cancer that puts the subject at risk for pleural or pulmonary metastases

Trial design

Treatments tested in this trial

  • E-Nose testing
  • Research blood

Treatment groups

20 Participants
are divided into 1 treatment group

Sponsors and collaborators

Memorial Sloan Kettering Cancer Center

Lead sponsor

UNIVERSITY CAMPUS BIO-MEDICO, ITALY

Collaborator