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This is a prospective, pilot, open-label, uncontrolled, non-randomized safety and effectiveness study of OCL 503 in men with BPH.
Prior to entering the study, all patients will undergo pre-study assessments including compliance with inclusion and exclusion criteria, laboratory assessments, IPSS, uroflowmetry, IIEF, and MRI pelvic imaging. Following conventional catheter angiography with cone-beam CT to confirm catheter placement and prostatic vasculature, each patient will undergo transarterial embolization with OCL 503. OCL 503 will be administered intra-arterially via microcatheter until there is stasis of blood flow.
Patient assessments include blood work, IPSS, uroflowmetry, IIEF, MRI and patient interviews conducted at 3 months, 6 months, and 12 months post embolization.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Prostate Artery Embolization | Experimental | Transarterial administration of OCL 503 to the arteries feeding the prostate. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Prostate artery embolization. | Device | Embolization of the prostatic vasculature with OCL 503 using a microcatheter. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Safety of OCL 503 as measured by Adverse Events reporting. | Measurement of device related adverse events post embolization of the prostatic vasculature, at 30 days. | 12 months |
| International Prostate Symptom Score (IPSS) | Measurement of IPSS at 12 months post embolization of the prostatic vasculature with OCL 503. | 12 months |
| Measure | Description | Time Frame |
|---|---|---|
| Tissue Response | Measurement in the change in size of the prostate by MRI at 12 months post embolization of the prostatic vasculature with OCL 503. | 12 months |
| Uroflowmetry | Measurement of Qmax, post-voiding bladder retention (PVR) at 12 months post embolization of the prostatic vasculature with OCL 503. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Richard Owen, MD | University of Alberta | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Alberta Hospital | Edmonton | Alberta | T6G 2B7 | Canada |
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| ID | Term |
|---|---|
| D011470 | Prostatic Hyperplasia |
| ID | Term |
|---|---|
| D011469 | Prostatic Diseases |
| D005832 | Genital Diseases, Male |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
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| 12 months |
| International Index of Erectile Function (IIEF) | Measurement of IIEF by questionnaire at 12 months post embolization of the prostatic vasculature using OCL 503. | 12 months |
| D052801 |
| Male Urogenital Diseases |