Last updated: October 12, 2022
Sponsor: HALO Diagnostics
Overall Status: Active - Recruiting
Phase
N/A
Condition
Traumatic Brain Injury
Vascular Diseases
Memory Loss
Treatment
N/AClinical Study ID
NCT05423860
HALO Dx 001
WIRB Pr. No.: 20213955
Ages 45-90 Male
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria: Treatment Naïve patients:
- Male, 45 years of age or older.
- Diagnosis of prostate adenocarcinoma.
- Clinical stage T1c or T2a.
- Gleason score of 7 (3+4 or 4+3) or less.
- Three or fewer biopsy cores with prostate cancer.
- PSA density not exceeding 0.375.
- One, two, or three tumor suspicious regions identified on multiparametric MRI.
- Negative radiographic indication of extra-capsular extent.
- Karnofsky performance status of at least 70.
- Estimated survival of 5 years or greater, as determined by treating physician.
- Tolerance for anesthesia/sedation.
- Ability to give informed consent.
- At least 6 weeks since any previous prostate biopsy.
- MR-guided biopsy confirmation of one or more MRI-visible prostate lesion(s) withGleason score of 7 (3+4 or 4+3) or less. Salvage candidates will be accepted upon physician referral.
Exclusion
Exclusion Criteria:
- Presence of any condition (e.g., metal implant, shrapnel) not compatible with MRI.
- Severe lower urinary tract symptoms as measured by an International Prostate SymptomScore (IPSS) of 20 or greater
- History of other primary non-skin malignancy within previous three years.
- Diabetes
- Smoker
Study Design
Total Participants: 2000
Study Start date:
March 16, 2022
Estimated Completion Date:
March 31, 2037
Study Description
Connect with a study center
Desert Medical Imaging
Indian Wells, California 92210
United StatesActive - Recruiting
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