CTRI/2017/10/010203已完成2 期
Acute Hemostasis following the use of the AQUABEAM® System for the treatment of Benign Prostatic Hyperplasia II - AHAII
PROCEPT BioRobotics0 个研究点目标入组 11 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 11
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. Subject has diagnosis of lower urinary tract symptoms due to benign prostatic enlargement causing bladder outlet obstruction
- •2. Prostate size >= 60 mL and <= 150 mL
- •3. IPSS score >= 12
- •4. Qmax <= 15ml/s
- •5. History of inadequate response, contraindication to or refusal of medical therapy
- •6. Patient is mentally capable and willing to sign a study-specific informed consent form
- •7. Patient is willing and able to comply with all study requirements
排除标准
- •1. BMI >= 42
- •2. Prostatitis treated with antibiotics within 1 year of enrollment
- •3. Significant renal impairment
- •4. Active infection, including urinary tract infection
- •5. Patients on anticoagulants (if medication cannot be stopped 5 days before and after procedure) or known coagulopathy or platelet disorder (except aspirin below 100mg/d)
- •6. History of gross haematuria
- •7. Known allergy to device materials
- •8. Any severe illness that would prevent complete study participation or confound study results
- •9. Serious concurrent medical conditions such as heart disease (e.g., myocardial infarction within 30 days, congestive heart failure â?? NYHA Class IV), pulmonary disease or uncontrolled diabetes.
- •10. Has had an open heart surgery, or cardiac arrest < 180 days prior to the date of informed consent
- •11. ASA III or higher
- •12. Participants using systemic immune-suppressants including corticosteroids; unable to withhold non-steroidal anti-inflammatory agents (NSAIDs, including aspirin greater or equal to 100mg) for 14 days prior to treatment
- •13. Known illicit substance abuse
- •14. Dementia or psychiatric condition that prevents the participant from completing required follow up
- •15. Contraindication to both general and spinal anesthesia
- •16. Participating in another investigational study that could affect responses to the study device
- •17. Subject is unwilling to accept a transfusion should one be required
研究者
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