POSLUMA PET Imaging for PI-RADS 3 Prostate Lesions
NCT07916311, Not applicable, Not yet recruiting, SimonMed Imaging
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | POSLUMA PET Imaging for PI-RADS 3 Prostate Lesions | ClinicalTrials.gov |
| NCT number | NCT07916311 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 130 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | SimonMed Imaging | ClinicalTrials.gov |
| Conditions | Prostate Cancer, PI-RADS 3 Prostate Lesion | ClinicalTrials.gov |
| Interventions | PET Imaging with Flotufolastat F 18 | ClinicalTrials.gov |
| First posted | 2026-11-04 | ClinicalTrials.gov |
| Last updated | 2026-11-04 | ClinicalTrials.gov |
Registered outcomes 8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Diagnostic accuracy of POSLUMA PET for clinically significant prostate cancer | From research PET imaging through histopathology review, up to approximately 6 weeks after the PET scan | Lesion-level area under the receiver operating characteristic curve for POSLUMA PET metrics, including SUVmax and PRIMARY score, using biopsy histopathology and clinically significant prostate cancer defined as Gleason score 7 or higher as the reference standard. | ClinicalTrials.gov |
| Secondary | Sensitivity of POSLUMA PET | From research PET imaging through histopathology review, up to approximately 6 weeks after the PET scan | Lesion-level sensitivity for detecting clinically significant prostate cancer using biopsy histopathology as the reference standard. | ClinicalTrials.gov |
| Secondary | Specificity of POSLUMA PET | From research PET imaging through histopathology review, up to approximately 6 weeks after the PET scan | Lesion-level specificity for detecting clinically significant prostate cancer using biopsy histopathology as the reference standard. | ClinicalTrials.gov |
| Secondary | Positive predictive value of POSLUMA PET | From research PET imaging through histopathology review, up to approximately 6 weeks after the PET scan | Positive predictive value for detecting clinically significant prostate cancer using biopsy histopathology as the reference standard. | ClinicalTrials.gov |
| Secondary | Negative predictive value of POSLUMA PET | From research PET imaging through histopathology review, up to approximately 6 weeks after the PET scan | Negative predictive value for detecting clinically significant prostate cancer using biopsy histopathology as the reference standard. | ClinicalTrials.gov |
| Secondary | Potential biopsy avoidance rate | At completion of biopsy histopathology review, up to approximately 6 weeks after the PET scan | Percentage of participants with low PSMA uptake who would be classified as potentially able to avoid biopsy under the study's exploratory imaging criteria. | ClinicalTrials.gov |
| Secondary | Missed clinically significant prostate cancer rate | At completion of biopsy histopathology review, up to approximately 6 weeks after the PET scan | Proportion of clinically significant prostate cancer cases associated with low PSMA uptake under the study's exploratory imaging criteria. | ClinicalTrials.gov |
| Secondary | Performance of a multivariable diagnostic model | After completion of imaging, biopsy, and histopathology data collection, through December 2028 | Model performance when combining PSMA PET metrics with clinical and imaging variables such as PSA, PSA density, free-to-total PSA ratio, ADC, lesion volume, and other protocol-specified variables. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)