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临床试验/NCT06657872
NCT06657872招募中不适用

Local Anesthesia With Schelin Catheter in Rezum Treatment: a Randomized Controlled Trial

Assistance Publique Hopitaux De Marseille1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2025年3月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
24
试验地点
1
主要终点
Comparison of the operating room occupancy time between the 2 groups

研究概览

简要总结

In a pilot study, water vapor therapy (RezumTM, Boston Scientific Corporation, Marlborough, MA) was proposed as a minimally invasive procedure for benign prostatic hyperplasia, but often requiring oral ± intravenous sedation or a transrectal prostatic block. Therefore, pain management during Rezum therapy remains a challenge and may lead to the use of pain control protocols and general anesthesia, limiting in some ways the concept of a minimally invasive ambulatory surgical approach. The Schelin® catheter (ProstaLund AB, Lund, Sweden), approved by the European Medicines Agency, is a device for injecting analgesic drugs directly into the prostate via the trans-urethral route, providing more effective local anesthesia and avoiding the need for transrectal route or general anesthesia. This catheter is therefore of crucial importance in offering to our patients an ultra-minimally invasive treatment, associated with a reduction in room occupancy time, outpatient surgery time, a procedure performed independently of the anesthesia team, and for the patient, an accelerated post-operative recovery. Our hypothesis is that the REZUM procedure under local anesthesia could be associated with a >20% reduction in operating room occupancy time compared to procedures performed under general anesthesia.

详细描述

Benign prostatic hyperplasia (BPH) is a common age-related pathology, affecting almost one in three men over the age of 50. It is responsible for voiding disorders in men, which can significantly impair quality of life. Briefly, drug treatment is currently used as first-line therapy; in the event of primary or secondary failure, surgery may be indicated. Over the past 25 years, a number of minimally invasive surgical therapies (MIST) have been developed for the treatment of male voiding disorders associated with BPH. MIST should enable rapid and lasting improvement in symptoms and quality of life, preservation of sexual function in contrast to conventional surgical techniques, rapid return to normal daily activity, and a minimal side-effect profile, thus enabling outpatient management. One of the many advantages of these techniques is to avoid the need for general anaesthesia, both for the growing cohort of elderly patients and for younger patients wishing to return to work quickly. In its pilot study, water vapor thermal therapy (RezumTM, Boston Scientific Corporation, Marlborough, MA) was proposed as a minimally invasive procedure, but often requiring oral ± intravenous sedation or a transrectal prostatic block. Therefore, pain management during Rezum therapy remains a challenge and may lead to the use of pain control protocols and general anesthesia, in some ways limiting the concept of a minimally invasive ambulatory surgery approach. In addition, the use of general anesthesia requires the presence of a dedicated anesthesia team, and adds to the burden of the patient journey (pre-operative anesthesia consultation, exposure to anesthetic drugs, passage to recovery room, slower post-operative recovery). From a surgical point of view, recourse to general anesthesia during Rezum treatment adds to an already saturated operative schedule, with significantly increased room occupancy time, for a Rezum therapy whose average operating time is 5 minutes. The Schelin® catheter (ProstaLund AB, Lund, Sweden), approved by the European Medicines Agency, is a device for injecting analgesic drugs directly into the prostate via the transurethral route, providing more effective local anesthesia and avoiding the need for transrectal or general anesthesia. This catheter is therefore of crucial use in offering our patients an ultra-minimally invasive treatment, which can be associated with a reduction in room occupancy time, time spent in outpatient surgery, a procedure performed independently of the anesthesia team, and for the patient, an accelerated post-operative recovery.

By delivering the Rezum treatment via the Schelin catheter, our hypothesis is a significant reduction (>20%) in room occupancy time in the operating room, associated with accelerated post-operative recovery for the patient.

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 80 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Patients referred for symptomatic benign prostatic hyperplasia (BPH)
  • Men between 45 and 80 years of age
  • IPSS > 13
  • Qmax <15 ml/s
  • Prostate volume between 30 and 80 g on ultrasound
  • Patient able to understand study details, benefits and risks
  • Patient able to give informed consent
  • Beneficiary of or affiliated to the French social security system
  • Patient having signed an informed consent form

排除标准

  • Patients with a history of prostate cancer
  • Patient with history of BPH surgery
  • Patients with a history of neurological bladder disease
  • Patient with history of urethral stricture
  • Patient with history of penile implants
  • Patient with history of pelvic irradiation
  • Patient with a symptomatic urinary tract infection in the 10 days prior to surgery
  • Presence of bladder stones on ultrasonography
  • Patient allergic to lidocaine 2% or any medication used in the pre-operative protocol (anxiolytics, analgesics and non-steroidal anti-inflammatory drugs)
  • Patient under guardianship or curatorship
  • Protected patient, deprived of liberty
  • Patient with a neurological and/or psychiatric disorder making it impossible to understand the terms of the study and to sign an informed consent form

研究组 & 干预措施

general anesthesia

Active Comparator

REZUM procedure under general anesthesia

干预措施: water vapor therapy under general anesthesia (Procedure)

Local anesthesia

Active Comparator

REZUM procedure under local anesthesia

干预措施: water vapor therapy under local anesthesia (Procedure)

结局指标

主要结局

Comparison of the operating room occupancy time between the 2 groups

时间窗: Visit 2: surgery

Operating room occupancy time during REZUM procedure

次要结局

  • Comparison of the quality of recovery after surgery between the 2 groups(24h after surgery)
  • Comparison of the pain post-surgery between the 2 groups(1 hour, 2 hours and 24 hours after surgery)
  • Success rate of the local anesthesia for the REZUM procedure(intraoperative)
  • Comparison of functional results between the 2 groups(3 months post-surgery)
  • Comparison of the average number of side-effects post-surgery between the 2 groups(30 days post-surgery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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