Phase
Condition
Lung Cancer
Non-small Cell Lung Cancer
Adenocarcinoma
Treatment
NovoTTF-200T System
Clinical Study ID
Ages > 22 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
The participant (or legally acceptable representative [LAR], if applicable) provideswritten informed consent for the study.
The participant is ≥22 years of age on the day of signing informed consent.
The participant has clinical stage 1A2, 1A3 or IB biopsy-proven lung ADC and iseligible for anatomical resection.
The participant has a lung nodule >1 cm and suspected lung ADC with a plan toundergo biopsy.
The participant with multiple nodules has one nodule that meets the criteria.
The participant has no history of prior malignancy in the chest or has undergonepotentially curative therapy with no evidence of that disease recurrence for 5 yearssince initiation of that therapy.
Exclusion
Exclusion Criteria:
Patients receiving therapy for concurrent active malignancy
Patients with a history of cardiac arrhythmias and/or pacemaker use
Patients with lung nodules <1cm
Patients with lung nodules that are pure ground glass opacities (GGOs) of any size
Patients with lung nodules that are <50% solid of any size
Study Design
Connect with a study center
Memorial Sloan Kettering Basking Ridge (Consent Only)
Basking Ridge, New Jersey 07920
United StatesSite Not Available
Memorial Sloan Kettering Monmouth (Consent Only)
Middletown, New Jersey 07748
United StatesSite Not Available
Memorial Sloan Kettering Bergen (Consent Only)
Montvale, New Jersey 07645
United StatesSite Not Available
Memorial Sloan Kettering Suffolk - Commack (Consent Only)
Commack, New York 11725
United StatesSite Not Available
Memorial Sloan Kettering Westchester (Consent Only)
Harrison, New York 10604
United StatesSite Not Available
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
New York, New York 10065
United StatesSite Not Available
Memorial Sloan Kettering Nassau (Consent Only)
Uniondale, New York 11553
United StatesSite Not Available

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