Holmium Laser Enucleation of Prostate(HOLEP) vs Greenlight(XPS) Laser Photoselective Vapo-Enucleation of Prostate(PVEP)
Primary Purpose
Benign Prostate Hyperplasia
Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
HOLEP
PVEP-XPS
Sponsored by
About this trial
This is an interventional treatment trial for Benign Prostate Hyperplasia focused on measuring LASER, BPH, Prostate surgery, HOLEP, Green light PVP
Eligibility Criteria
Inclusion Criteria:
- 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) > 15.
- 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).
Exclusion Criteria:
- 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.
Sites / Locations
- Royal victoria hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
HOLEP
PVEP/XPS
Arm Description
HOLEP In the first arm, holmium laser enucleation of the prostate will be done
PVEP/XPS green light photoselective Vapo-Enucleation of prostate using XPS 180W machine will be used in the second arm
Outcomes
Primary Outcome Measures
change in urine flow parameters
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
Secondary Outcome Measures
TIME TO CATHETER REMOVAL, HOSPITAL STAY
At first postoperative day; the catheter will be removed for trial voiding Patient will be discharged from the hospital as soon as possible (same day or once urine color is normalized)
the need for redo surgery
The need for re-operation in the fist year will be assessed
Full Information
NCT ID
NCT01494337
First Posted
December 5, 2011
Last Updated
August 25, 2014
Sponsor
Royal Victoria Hospital, Canada
Collaborators
McGill University
1. Study Identification
Unique Protocol Identification Number
NCT01494337
Brief Title
Holmium Laser Enucleation of Prostate(HOLEP) vs Greenlight(XPS) Laser Photoselective Vapo-Enucleation of Prostate(PVEP)
Official Title
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
Study Type
Interventional
2. Study Status
Record Verification Date
August 2014
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
March 2014 (Actual)
Study Completion Date
April 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Royal Victoria Hospital, Canada
Collaborators
McGill University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
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
Detailed Description
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.
Patients will be seen in follow-up at 2 weeks, 1, 3, 6, and 12 months. The parameters to be assessed at each time point are listed below. As can be seen from the table, the most important parameters will be changes in voiding symptoms and uroflowmetry over time. Some validated questionnaires will be utilized to assess the patients' sexual function both at base line and at different follow-up visits. Different aspects of the sexual function will be analysed, partner's feedback will be addressed by a special questionnaire.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Benign Prostate Hyperplasia
Keywords
LASER, BPH, Prostate surgery, HOLEP, Green light PVP
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
108 (Actual)
8. Arms, Groups, and Interventions
Arm Title
HOLEP
Arm Type
Active Comparator
Arm Description
HOLEP In the first arm, holmium laser enucleation of the prostate will be done
Arm Title
PVEP/XPS
Arm Type
Active Comparator
Arm Description
PVEP/XPS green light photoselective Vapo-Enucleation of prostate using XPS 180W machine will be used in the second arm
Intervention Type
Procedure
Intervention Name(s)
HOLEP
Other Intervention Name(s)
Holmium Laser Enucleation of The Prostate
Intervention Description
USING HOLMIUM LASER, the prostate adenoma will be enucleated and removed into small pieces
Intervention Type
Procedure
Intervention Name(s)
PVEP-XPS
Other Intervention Name(s)
Photoselective Vapo-Enucleation of prostate(PVEP)
Intervention Description
Greenlight laser will be used with high power setting for selective vaporization of the prostate adenoma, using 180 watt XPS laser machine
Primary Outcome Measure Information:
Title
change in urine flow parameters
Description
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
Time Frame
one, 4 and 12 months postoperative
Secondary Outcome Measure Information:
Title
TIME TO CATHETER REMOVAL, HOSPITAL STAY
Description
At first postoperative day; the catheter will be removed for trial voiding Patient will be discharged from the hospital as soon as possible (same day or once urine color is normalized)
Time Frame
1 day post operative
Title
the need for redo surgery
Description
The need for re-operation in the fist year will be assessed
Time Frame
1 year
10. Eligibility
Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
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) > 15.
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).
Exclusion Criteria:
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mostafa M Elhilali, Professor
Organizational Affiliation
McGill University Health Centre/Research Institute of the McGill University Health Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal victoria hospital
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3A 1A1
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
25261801
Citation
Elshal AM, Elkoushy MA, El-Nahas AR, Shoma AM, Nabeeh A, Carrier S, Elhilali MM. GreenLight laser (XPS) photoselective vapo-enucleation versus holmium laser enucleation of the prostate for the treatment of symptomatic benign prostatic hyperplasia: a randomized controlled study. J Urol. 2015 Mar;193(3):927-34. doi: 10.1016/j.juro.2014.09.097. Epub 2014 Sep 28.
Results Reference
derived
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Holmium Laser Enucleation of Prostate(HOLEP) vs Greenlight(XPS) Laser Photoselective Vapo-Enucleation of Prostate(PVEP)
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