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临床试验/NCT05543200
NCT05543200招募中不适用

A Global Registry of Treatments and Outcomes for Benign Prostatic Hyperplasia

Société Internationale d'Urologie33 个研究点 分布在 22 个国家目标入组 7,500 人开始时间: 2023年3月13日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
7,500
试验地点
33
主要终点
Complications (including incontinence)

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Primary diagnosis of BPH with LUTS with prescribed medical treatment or surgical intervention

排除标准

  • Non-symptomatic BPH
  • No treatment prescribed for BPH

研究组 & 干预措施

All Participants

All men who have a primary diagnosis of BPH with LUTS that are prescribed BPH medications or a surgical intervention.

结局指标

主要结局

Complications (including incontinence)

时间窗: 36 months

Type and Clavien grade incidences across all surgical interventions.

Post-Void Residual (PVR)

时间窗: 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)

时间窗: 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)

时间窗: 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.

次要结局

  • 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)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (33)

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