Prospective, Multi-Center Study of the ClariCore Optical Biopsy System in Patients Undergoing Transrectal Ultrasound (TRUS)-Guided Prostate Biopsy for Real-Time Tissue Evaluation
试验速览
- 阶段
- 不适用
- 入组人数
- 325
- 试验地点
- 10
- 主要终点
- Validation of the tissue classification algorithm
研究概览
简要总结
The purpose of this study is to demonstrate the effectiveness and safety of the ClariCore System in obtaining prostate biopsies with device feedback that provides real-time tissue classification.
详细描述
The purpose of this study is to collect information on prostate biopsies using the ClariCore System. The ClariCore System is designed to improve how the biopsies are being collected from the prostate by using light sensors (fiber optics) that can see changes in the prostate tissue. Researchers will study the information collected from the light sensors to study a method that has been developed to tell the difference between normal and suspicious (possibly cancerous) prostate tissue during the biopsy. This information will be given to the doctor in real-time. From this study, researchers hope to learn if this method can tell the difference between normal and suspicious prostate tissue, and if this can improve the evaluation of prostate tissue (biopsies).
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 22 Years 至 —（Adult, Older Adult）
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Males > 22 years old
- •Patient scheduled for TRUS-guided prostate biopsy based on standard of care urologic requirements to assess for tissue malignancy (abnormal Digital Rectum Examination, Prostate Specific Antigen kinetics, age, ethnicity, family history, etc.)
- •Enrolling physician must have expectation that prostate dimensions will meet minimum prostate volume and height requirements that will be evaluated at start of biopsy procedure (i.e., Prostate volume > 20cc and height at least 22mm)
- •Patient signs an Institutional Review Board approved, Informed Consent form to participate in the study prior to any study mandated determinations or procedure
排除标准
- •Any anatomical or co-morbidity contraindications to TRUS prostate biopsy
- •Acute painful perianal disorder (i.e. rectal abscess)
- •Symptomatic, acute prostatitis
- •Surgical absence of a rectum or the presence of a rectal fistula
- •Patient has systemic infection or evidence of any surgical site infection (superficial or organ space), including active urinary tract infection
- •Previous prostate intervention [Transurethral Prostatectomy (TURP) (bipolar, monopolar, laser)], Transurethral Microwave Thermotherapy (TUMT), High-Intensity Focused Ultrasound (HIFU), Cryo, Rezum, Urolift], not including previous prostate biopsy
- •Current use of blood thinning agents for medical comorbidity which prohibits the cessation of use as typically required per standard of care (SOC) or history of a bleeding disorder (e.g. coagulopathy)
- •Prior pelvic irradiation
- •Actively receiving therapy for the treatment of cancer (except for patients on 5-alpha reductase inhibitors, or non-melanoma skin cancers that are managed nonsystemically)
- •Actively receiving intravesical therapy or within 6 months of treatment for bladder cancer
- •Patient has compromised immune system
- •Active inflammatory bowel disease within the last 6 months
- •Any condition, or history of illness or surgery that, in the opinion of the Investigator, might confound the results of the study or pose additional risks to the patient (e.g. significant cardiovascular conditions or allergies)
- •Patient is not likely to comply with the protocol or follow up evaluation
- •Patient is participating in a clinical trial of another investigational drug or device that may impact participation in this clinical study
- •Patient is unable to provide legal Informed Consent
研究组 & 干预措施
ClariCore System
ClariCore System study designed to obtain prostate biopsies utilizing real-time tissue classification with the ClariCore Optical Biopsy System.
干预措施: ClariCore Optical Biopsy System (Device)
结局指标
主要结局
Validation of the tissue classification algorithm
时间窗: At time of procedure
Correlate histopathology of tissue biopsy core samples with the tissue classification algorithm results obtained at the time of the procedure to validate the tissue classification algorithm.
次要结局
- Cancer Detection Rate(At time of procedure)
- Sensitivity and Specificity(At time of procedure)