UnknownNot Applicable

Evaluation of the NV-VPAC1 Prostate Cancer (PCa) Urine Diagnostic Test in Subjects With Biopsy-confirmed Prostate Cancer, Benign Prostatic Hypertrophy, or Bladder/Kidney Stones.

United States45 participantsStarted 2018-10-16

Plain-language summary

This is a double-blind, study to evaluate the performance of NV-VPAC1 PCa Urine Diagnostic Test in three distinct populations being treated at the Intermountain Urology Clinic. The first population (positive control) is comprised of men with biopsy-confirmed PCa who are scheduled for prostatectomy. The second population (negative control) is comprised of men with benign prostatic hypertrophy (BPH) who are scheduled for transurethral resection of the prostate (TURP). The third population (negative control) is comprised of men or women with bladder/kidney stones who are scheduled for a cystoscopy.

Who can participate

Age range18 Years – 80 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Subjects with prostate cancer Inclusion Criteria: * Males 18-80 years of age * Biopsy-confirmed prostate cancer * Scheduled within 2 weeks for prostatectomy * Signed informed consent Exclusion Criteria: * Presence or history of another cancer diagnosis, with the exception of certain skin cancers * Currently treated with finasteride (Proscar®, Propecia®), dutasteride (Avodart®) or anti-androgen therapy (Lupron®) * Participated in a clinical study with an investigational drug within 2 weeks of the screening visit. Subjects with benign prostatic hypertrophy Inclusion Criteria: * Males 18-80 years of age * Diagnosis of BPH made by clinical symptoms (e.g., enlarged prostate, dribbling urine stream, frequent and urgent urination) * Scheduled within 2 weeks for TURP * Signed informed consent Exclusion Criteria: * Presence or history of any cancer diagnosis, with the exception of certain skin cancers * Currently treated with finasteride (Proscar®, Propecia®) or dutasteride (Avodart®) * Participated in a clinical study with an investigational drug within 2 weeks of the screening visit. Subjects with bladder/kidney stones Inclusion Criteria: * Males or females 18-80 years of age * Diagnosed with bladder/kidney stones * Scheduled within 2 weeks for cystoscopy * Signed informed consent Exclusion Criteria: * Presence or history of any cancer diagnosis, with the exception of certain skin cancers * Participated in a clinical study with an investigational drug within 2 weeks of…

What they're measuring

Degree of association of the presence of orange fluorescent positive cells shed in voided urine and lack of association of orange fluorescent positive cells in men diagnosed with BPH or in individuals with bladder/kidney stones

Timeframe: 6 months

Trial details

NCT IDNCT03630926

SponsorIntermountain Health Care, Inc.

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2019-08