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Detecting Recurrent Prostate Cancer With 11C-choline Positron Emission Tomography

Detecting Recurrent Prostate Cancer With 11C-choline Positron Emission Tomography: An Expanded Access Study

Status
NO_LONGER_AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT02531672
Enrollment
Unknown
Registered
2015-08-24
Start date
Unknown
Completion date
Unknown
Last updated
2020-06-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer, Recurrent Prostate Cancer

Keywords

11C-choline, Positron Emission Tomography, 15-117

Brief summary

The purpose of this study is to use a new imaging drug called 11C-choline that is used with a PET/CT scan to see prostate cancer when it cannot be seen well on other scans, such as bone scans, CT or MRI.

Interventions

DEVICEPET/CT Scan

Sponsors

Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient must have biopsy-proven adenocarcinoma of the prostate initially treated with curative intent (surgery and radiation therapy are most common treatments but other treatments are also eligible). * Biochemical recurrence defined as any of the following: 1. PSA ≥ 0.2 ng/mL in at least two sequential tests for patients treated with surgery. 2. PSA ≥ 0.2 ng/mL above the post therapy nadir for patients treated with radiation therapy, brachytherapy or cryotherapy. 3. PSA ≥ 0.2 ng/ml above the most recent therapy nadir for patients who have received additional treatment in the recurrent setting * Patient must have undergone standard-of-care restaging that does not clearly identify site(s) of active disease, or such prior studies must show equivocal findings for which further work-up is considered necessary to make clinical decision. Standard staging examinations may include one or more of the following: CT or MRI, bone imaging (either Tc-99m bisphosphonate scintigraphy MDP or F-18 sodium fluoride PET), FDG PET, or In-111 capromab pendetide scintigraphy no older than 3 months of consent date. * Age ≥ 18 years. * Patient must be able to tolerate PET/CT imaging. * Patient must be able to understand and willing to sign a written informed consent document.

Exclusion criteria

* Patient must not have claustrophobia that would preclude PET/CT imaging or other contraindications to CT imaging.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026