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OTHERClinicalTrials.govClinical trialPhase 2Not yet recruiting

Effectiveness of Posluma PET Scan for Post-Treatment Monitoring of Prostate Cancer

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Official record

Identifier
NCT07733908
Recruiting locations
Locations are not included in the offline baseline for this record. Open the official record to see the current site list.
Interventions studied
Posluma PET
Lead sponsor
Aditya Bagrodia
Target enrolment
22 participants
Study type
INTERVENTIONAL
Phase
Phase 2
Status
Not yet recruiting
First posted
Jul 29, 2026
Last updated on the registry
Aug 14, 2026
Age
18 Years
Sex
MALE
Study contact
The official record lists a study contact. Contact details are published there and are intentionally not copied to this page.
Eligibility criteria

Reproduced verbatim from the official record. Eligibility is decided by the study team, never by this page.

Inclusion Criteria:

1. Diagnosis: Histologically confirmed PCa.
2. Risk Profile: Intermediate-risk , organ-confined PCa
3. Eligibility for Focal Therapy: Determined to be an appropriate candidate for focal therapy based on clinical evaluation.
4. Age: 18 years or older.
5. Life Expectancy: Expected survival of at least 10 years.
6. Informed Consent: Ability to understand and willingness to sign the informed consent form.

Exclusion Criteria:

1. Previous Treatment: Prior treatment for PCa, including radiation therapy, chemotherapy, focal therapy, or androgen deprivation therapy.
2. Severe Comorbid Conditions: Presence of severe comorbid conditions that may interfere with study participation, such as uncontrolled cardiovascular, renal, hepatic, or metabolic diseases.
3. Contraindications to Imaging: Known hypersensitivity to components of the Posluma PSMA radiotracer, or inability to undergo PET or MRI imaging due to medical or anatomical constraints (e.g., severe claustrophobia, metallic implants incompatible with MRI).
Indexed under
Prostate Cancer