New tech aims to sharpen lung cancer radiation targeting
NCT ID NCT02434809
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new computer program that reduces blurring in CT scans used during lung cancer radiation therapy. The goal is to help doctors better locate tumors and track small markers placed in the lungs. About 17 adults with lung cancer who are already scheduled for radiation therapy will take part. The study focuses on improving imaging accuracy, not on directly treating the disease.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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17 people
The number who actually took part.
- Start date
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Apr 2015
- Expected to finish
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Apr 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Histologic proof of malignancy suitable for thoracic radiation therapy * Patient is planning to undergo radiation therapy for primary or recurrent malignancies of the lung or metastatic malignancies to the lung. * Age ≥ 18 years old * Karnofsky Performance Status ≥ 60% * At least part of the tumor must be visible as observed in a diagnostic or planning CT. * Able to have bronchoscopic placement of Calypso transponders as confirmed on a recent (within the past 8 weeks) CT scan. Exclusion Criteria: * Patients with clinically significant active infections. * Bronchiectasis in the region of the intended implantation. * History of hypersensitivity to nickel. * Other medical condition or laboratory value that would, at the discretion of the investigator, preclude the patient from participation in this clinical study. * Deemed unable to safely undergo or tolerate flexible bronchoscopy as per institutional guidelines * Unable to tolerate anesthesia or sedation * Enrolled in any other clinical studies the investigator believes to be in conflict with this investigation. * Female patients who are pregnant or nursing Exclusion criteria for Calypso transponders: * Implants in the chest region that contain metal or conductive materials (e.g., metal implants, rods, or plates) which Calypso Medical considers will interfere with the Calypso System's electromagnetic localization. * Active implanted devices, such as pacemakers, defibrillators, and drug infusion pumps since the effects of the Calypso System operation on these devices are unknown. * Patients whose lung tumors are being monitored by MR imaging as part of standard clinical care. Implantation of transponders will degrade MR images. * Posterior lesions that would be \>19 cm distance from Calypso detector plate.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
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Memorial Sloan Kettering Cancer Commack
Commack, New York, 11725, United States
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Memorial Sloan Kettering Westchester
Harrison, New York, 10604, United States
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Other studies related to the condition(s) this trial covers.
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