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临床试验/NCT07749794
NCT07749794尚未招募不适用

Hydrodissection-Assisted Bipolar Prostatic Enucleation-Enucleoresection With Subcapsular Injection of Diluted Norepinephrine-Methylene Blue Mixture Versus Conventional Bipolar Prostatic Enucleation-Enucleoresection: A Prospective Randomized Comparative Study

Benha University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2026年8月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
100
试验地点
1
主要终点
Intraoperative Blood Loss

研究概览

简要总结

This prospective randomized study will compare two surgical techniques for treating benign prostatic hyperplasia. Participants will be assigned to either hydrodissection-assisted bipolar prostatic enucleation-enucleoresection with transrectal ultrasound-guided subcapsular injection of diluted norepinephrine and methylene blue or conventional bipolar prostatic enucleation-enucleoresection without injection.

The injected mixture is intended to separate the enlarged prostatic tissue from the surgical capsule and reduce bleeding during surgery. The study will evaluate whether the hydrodissection-assisted technique improves operative conditions, surgical outcomes, postoperative recovery, urinary symptoms, and urinary flow compared with the conventional technique.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

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

  • Benign prostatic hyperplasia.
  • Prostate volume greater than 60 cc as measured by transrectal ultrasonography.
  • Moderate-to-severe lower urinary tract symptoms, defined as an International Prostate - Symptom Score of 12 or higher.
  • Failure of or poor response to medical management.

排除标准

  • History of prostate cancer or suspicious findings on prostate biopsy.
  • Active urinary tract infection.
  • Severe cardiovascular, pulmonary, or other systemic comorbidities that contraindicate surgery.
  • Previous prostate surgery, including transurethral resection of the prostate or open prostatectomy.
  • Chronic urinary retention associated with neurogenic bladder. Hypersensitivity to norepinephrine or methylene blue.

研究组 & 干预措施

Hydrodissection-Assisted Bipolar Prostatic Enucleation-Enucleoresection

Experimental

Participants will undergo transrectal ultrasound-guided subcapsular injection of a diluted norepinephrine-methylene blue mixture to produce hydrodissection between the prostatic adenoma and surgical capsule, followed by bipolar prostatic enucleation-enucleoresection. Standard postoperative bladder irrigation, catheter management, and follow-up will be provided.

干预措施: Hydrodissection-Assisted Bipolar Prostatic Enucleation-Enucleoresection (Procedure)

Conventional Bipolar Prostatic Enucleation-Enucleoresection

Active Comparator

Participants will undergo conventional bipolar prostatic enucleation-enucleoresection without subcapsular injection or hydrodissection. Standard postoperative bladder irrigation, catheter management, and follow-up will be provided.

干预措施: Conventional Bipolar Prostatic Enucleation-Enucleoresection (Procedure)

结局指标

主要结局

Intraoperative Blood Loss

时间窗: Intraoperatively

The estimated volume of blood lost during the operative procedure will be recorded in milliliters and compared between the hydrodissection-assisted and conventional groups.

次要结局

  • Operative Time(Intraoperatively)
  • Enucleated Prostatic Tissue Weight(Immediately after tissue retrieval, intraoperatively)
  • Length of Hospital Stay(From completion of surgery until hospital discharge, assessed up to 7 days)
  • Urethral Catheterization Duration(From completion of surgery until catheter removal, assessed up to 7 days)
  • Change in Maximum Urinary Flow Rate(At baseline and at 1, 3, and 6 months after surgery)
  • Change in Post-Void Residual Urine Volume(At baseline and at 1, 3, and 6 months after surgery)
  • Change in International Prostate Symptom Score(At baseline and at 1, 3, and 6 months after surgery)
  • Incidence of Postoperative Complications(At 1, 3, and 6 months after surgery)
  • Incidence of Intraoperative Complications(Intraoperatively)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Saad ali saad salama

Lecturer of Urology

Benha University

研究点 (1)

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