A Global Registry of Treatments and Outcomes for Benign Prostatic Hyperplasia
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Enrollment
- 7,500
- Locations
- 30
- Primary Endpoint
- Complications (including incontinence)
Study Overview
Brief Summary
Benign prostatic hyperplasia (BPH) is one of the most common performed surgical procedures in urology. Over the past few decades there have been an increasing development of newer surgical treatment options. Additionally, the outcome parameters for BPH treatments have been standardized. While data are available for the initial pivotal studies, post-market release data are lacking. Under the umbrella of uCARE, we have started a prospective, ongoing international registry for recording demographics and outcomes for patients undergoing surgical treatments for BPH.
Detailed Description
Due to a growing and aging population, cases of benign prostatic hyperplasia (BPH) have been on a steady rise. Studies show that by age 80, 90% of men experience BPH. (Garraway, Lee, Collins, 1991) Thus, treatment of BPH is one of the most performed surgical procedures in urology. Over the past few decades there have been an increasing development of newer surgical treatment options. Additionally, the outcome parameters for BPH treatments have been somewhat standardized. The purpose of this study is to create an ongoing prospective registry to record demographic data and clinical outcomes after medical therapy or different surgical interventions for BPH. The specific aims of the registry are to analyze demographic patterns and baseline characteristics of men undergoing surgical and medical treatments for BPH, to assess global practice patterns for various surgical and medical treatments of BPH, and to assess key outcomes for uni- and multi-modal treatments of BPH.
The ongoing global registry will provide important baseline data, functional outcomes, and complications following medical and/or surgical intervention for men with symptomatic BPH. The intention of the registry is to provide real world usage data that may be used for future investigations. It will allow providers to identify areas of interest, areas of unusually low usage or areas of unusual preference on a global scale. It will also shed light on global preferences for unimodal or multimodal approaches to treatments.
The registry has been developed using novel database technology, providing an easy-to-use user interface, which enables future creation of patient portals and Electronic Medical Record (EMR) integration.
As this is not an experimental setting, there will be no interventions made on behalf of the registry.
This is a prospective longitudinal ongoing registry. The study will include medical records of all men ≥18 years old who have a primary diagnosis of BPH with Lower Urinary Tract Symptoms (LUTS) that are prescribed BPH medications, or a surgical intervention. Data extraction includes baseline data, peri-operative data, and follow-up data. Baseline data includes validated patient reported outcome tools, including International Prostate Symptom Score (IPSS), Sexual Health Inventory for Men (SHIM), Male Sexual Health Questionnaire - Ejaculatory Dysfunction (MSHQ-EjD), as well as Quality of Life (QoL), maximum flow rate (Qmax), Post-void residual (PVR), Prostate Specific Antigen (PSA), and Testosterone. Complications such as Bleeding, Urinary Tract Infection (UTI), Incontinence, Stricture, Retrograde ejaculation, and Erectile Dysfunction (ED) are also tracked from Baseline through Follow-up.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- Male
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Primary diagnosis of BPH with LUTS with prescribed medical treatment or surgical intervention
Exclusion Criteria
- •Non-symptomatic BPH
- •No treatment prescribed for BPH
Arms & Interventions
All Participants
All men who have a primary diagnosis of BPH with LUTS that are prescribed BPH medications or a surgical intervention.
Outcomes
Primary Outcomes
Complications (including incontinence)
Time Frame: 36 months
Type and Clavien grade incidences across all surgical interventions.
Post-Void Residual (PVR)
Time Frame: 36 months
Comparison of mean PVR change between baseline and at each follow-up during the course of the study.
International Prostate Symptom Score (IPSS)
Time Frame: 36 months
Comparison of mean IPSS score change between baseline and at each follow-up during the course of the study. The scale goes from 0 (Mild) to 35 (Severe).
Quality of Life (QoL)
Time Frame: 36 months
Comparison of mean QoL score change between baseline and at each follow-up during the course of the study. The scale is a single question which ranges from 0 to 6, with higher numbers indicating a worse quality of life.
Secondary Outcomes
- Sexual Health Inventory for Men (SHIM)(36 months)
- Male Sexual Health Questionnaire Ejaculatory Dysfunction (MSHQ-EjD)(36 months)
- Prostate Volume (cc)(36 months)
- Qmax(36 months)
