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临床试验/NCT01494337
NCT01494337已完成4 期

Randomized Study Comparing Holmium Laser Enucleation of the Prostate (HOLEP) Versus Greenlight (XPS) Laser Photoselective Vapo-Enucleation of Prostate(PVEP) in the Management of Infravesical Obstruction Secondary to BPH

Royal Victoria Hospital, Canada2 个研究点 分布在 1 个国家目标入组 108 人开始时间: 2012年1月1日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
108
试验地点
2
主要终点
change in urine flow parameters

研究概览

简要总结

The investigators are now proposing to compare two laser techniques for treating Benign prostate hyperplasia (BPH); Holmium Laser Enucleation of the Prostate (HOLEP) versus (greenlight) XPS which is a recently available technology in our center and is more efficient hence our choice to include patients with any size prostate. This will confirm whether the two techniques are equivalent in efficacy and safety independent of size as well as cost. The two techniques are available world wide as standard of care

详细描述

Patients with lower urinary tract symptoms (LUTS) secondary to bladder outlet obstruction from BPH seen through the outpatient clinic in the urology department will be assessed to see if the patient satisfies all inclusion and exclusion criteria. Patients who are meeting these criteria will be asked to participate in this randomized comparison study. If they agree they will be provided with an informed consent form which they can take home with them. The randomization process will be performed using computer-generated simple random tables in a 1:1 ratio. Study participants will be enrolled randomized, and the appropriate surgery scheduled. Procedures will be performed on an outpatient basis whenever possible.

All surgeries will be performed under a spinal or general anaesthesia. In case of coexisting vesical stone, Holmium laser cystolithotripsy will be done first regardless the type of next procedure for the prostate. Both HOLEP and greenLight (XPS) laser vaporization of the prostate begins with the insertion of a resectoscope transurethrally. Examination of the lower urinary tract is performed and holmium laser fiber is used to enucleate (HOLEP) or to vaporize [greenLight (XPS)] the obstructing prostatic tissue using the Moxy fibre until the surgical capsule is reached. After treatment, the prostatic fossa will be examined for hemostasis and if adequate, a 22 french Foley catheter will be inserted. Patients will then be sent to the post-anaesthetic recovery room.

Once awake, the patient could have the catheter removed with a voiding trial if the urine is judged to be sufficiently clear and the surgeon is comfortable about early catheter removal. Those patients able to void will be sent home without catheter. Those patients unable to void or the surgeon decides to keep the catheter for 24 hours will be either sent home with a catheter to be removed the next day or hospitalized overnight.

Finally, those patients with multiple medical problems or with postoperative bleeding requiring bladder irrigation will be kept overnight with a trial of voiding attempted the next morning if the urine is clear.

Intraoperative and early postoperative parameters of interest will be recorded and compared between groups. These parameters include the total procedure time, total laser energy used, cost of disposables including the number of laser fibers per case, number of bags of irrigant per case, urethral catheterization time, length of hospital stay, subjective assessment of hemostasis during each laser procedure, objective assessment of changes in serum electrolytes and hematocrit and thorough recording of all complications.

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

性别
Male
接受健康志愿者

入选标准

  • Ability to give informed consent.
  • Lower urinary symptoms (LUTS) secondary to bladder outlet obstruction from BPH.
  • Failed medical treatment of BPH.
  • International prostate symptom scores (IPSS) >
  • Peak urinary flow rate (Qmax) < 15 ml/sec.
  • Preoperative TRUS (transrectal ultrasound) size of the gland (from 40 to 150 cc).
  • Patients in retention secondary to BPH (with cystometrogram (CMG) confirming adequate detrusor pressure if the bladder capacity at time of catheterization is in excess of 1000 ml).

排除标准

  • Inability to give informed consent.
  • Patient who have a neurological disorder which might affect bladder function as cerebrovascular stroke, Parkinson disease.
  • Active urinary tract infection.
  • Presence of active bladder cancer (within the last 2 years).
  • Known cancer prostate patients will be excluded preoperatively on the basis of digital rectal examination, prostate specific antigen level, and TRUS imaging followed by prostate biopsies if necessary.

结局指标

主要结局

change in urine flow parameters

时间窗: one, 4 and 12 months postoperative

change in urine flow parameters; IPSS= international prostate symptom score QOL= quality of life score PVR= post voiding residual urine Q-MAX= maximal flow rate

次要结局

  • TIME TO CATHETER REMOVAL, HOSPITAL STAY(1 day post operative)
  • the need for redo surgery(1 year)

研究者

发起方
Royal Victoria Hospital, Canada
申办方类型
Other
责任方
Principal Investigator
主要研究者

Mostafa Elhilali

clinical professor

Royal Victoria Hospital, Canada

研究点 (2)

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