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临床试验/NCT06373419
NCT06373419招募中不适用

Thulium Fiber Laser (TFL) Versus MOSES Holmium Laser in the En-bloc Resection of Bladder Tumors: A Randomized Controlled Clinical Study

Thunder Bay Regional Health Research Institute2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2023年10月16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
100
试验地点
2
主要终点
Incidence of inconclusive pathology

研究概览

简要总结

The goal of this randomized clinical trial is to determine if there is difference in pathological and clinical outcomes between MOSES and TFL in the transurethral laser enucleation of bladder tumors.

The main question it aims to answer is:

Is there a difference in pathological and clinical outcomes between MOSES Holmium and Thulium Fiber Laser (TFL) in the transurethral laser enucleation of bladder tumors?

Participants will randomized to either TFL of MOSES arm for their bladder resection procedure.

详细描述

An estimated 12,500 Canadians are diagnosed with bladder cancer each year. Diagnosis and treatment involve transurethral (through the urethra) resection of tumor or tissue called the TURBT procedure. This procedure yields excellent results and minimal morbidity and mortality but has a high recurrence rate, difficulties in the pathologic interpretation of the specimen (due to cautery effect), and procedure-related complications (excessive bleeding, bladder perforation, bowel injury, and inadvertent extensive injury to urethra) that may delay treatments such as chemotherapy which would further impact oncologic outcomes. With the advancement of technology, new methods of transurethral tumor removal have emerged, such as the use of laser energy. Using laser energy, the tumour is resected in one piece, whereas the TURBT approach requires breaking the tumor into pieces. This allows for better pathology analysis that can determine treatment pathways for the patient, as well as reduces the risk of complications. The standard lasers used have been the MOSES Holmium laser and the Thulium Fiber Laser (TFL).

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
All
接受健康志愿者

入选标准

  • Over 18 years of age at the time of enrollment.
  • Patients presented with visual criteria suggesting bladder tumor by outpatient cystoscopy will be legible for inclusion.

排除标准

  • Tumors deemed not eligible for laser resection as determined by the Urologist e.g. obvious muscle-invasive or metastatic at presentation
  • Synchronous either urethral tumors or upper urinary tract tumor
  • History of Carcinoma in situ
  • Contracted bladder

结局指标

主要结局

Incidence of inconclusive pathology

时间窗: 1 day post-procedure

Incidence of inconclusive pathology due to specimen artifact

Presence of muscularis propria

时间窗: 1 day post-procesure

Presence of muscularis propria (bladder muscle cells) in the pathology sample of the bladder tumour

次要结局

  • Total procedural time(Intraoperative)
  • Total blood loss(6 hours post-procedure)
  • Total operative time(Intraoperative)
  • Lasing time(Intraoperative)
  • Tumor-free rate (TFR)(6 to 12 weeks post-procedure)
  • Rate of complications(4 weeks post-procedure)
  • Number of recurrences(12 weeks post-procedure)
  • Number of inconclusive pathology(1 day post-procedure)
  • Total energy used(Intraoperative)
  • Frequency and severity of peri-operative complications(Intraoperative)

研究者

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

Ahmed Zakaria Ahmed

Urologist

Thunder Bay Regional Health Research Institute

研究点 (2)

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