Cancer imaging study pulled before starting
NCT ID NCT04488224
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to test a new device that rotates patients horizontally to take CT images for guiding radiation therapy in cancer patients. It was designed for adults with certain cancers, but the trial was withdrawn before enrolling anyone. The goal was to see if the images were good enough for treatment planning.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Expected to start
-
Sep 2025
An estimate. Start dates often move.
- Finished
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Dec 2025
- 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
-
18 years and older
- Sex
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Anyone
- Healthy volunteers
-
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: 1. Cancer patients that are receiving radiation therapy that are able to be imaged with the Nano-X PRS with one of the following tumour sites: 1. in the head/neck region 2. in the chest/abdomen/pelvic region with fast CBCT used for standard of care image guidance and is aged 60 years or older 3. in the chest/abdomen/pelvic region not receiving CBCT for standard of care image guidance and is aged 70 years or older 4. diagnosis of lung cancer with stage II-IV 2. ≥18 years of age 3. ECOG Performance Status 0-2 4. Must be able to communicate fluently in English to: i. Receive instructions from operators of the PRS for safety entering and leaving the Patient Rotation System and required conduct during the during the rotation session, and ii. Communicate their level of comfort or distress to operators of the equipment. 5. Signed, written informed consent or approved alternative, non-contact method for informed consent. Exclusion Criteria: 1. Pregnant women 2. Patients for whom attaining informed consent would not be possible, including mentally impairment 3. Patients with severe vertigo or recent a diagnosis of Benign Paroxysmal Positioning Vertigo.
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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.
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Other studies related to the condition(s) this trial covers.
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