search
Back to results

Urodynamic Evaluation of Disobstrucitve Power of Aquablation VS Laser Techniques

Primary Purpose

Benign Prostatic Hyperplasia (BPH)

Status
Unknown status
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
aquablation
holep
pvp
Sponsored by
University of Bari
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Benign Prostatic Hyperplasia (BPH)

Eligibility Criteria

40 Years - 90 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • moderate-to-severe lower urinary tract symptoms (IPSS ≥ 12)
  • poor efficacy or tolerance to medical therapy for BPH
  • transrectal ultrasound prostate volume between 30 and 120 ml
  • ability to express written informed consent.

Exclusion Criteria:

  • previous surgical treatments for BPH
  • indwelling bladder catheter or clean intermittent catheterization
  • bladder stones
  • severe detrusor hypocontractility (BCI <50) or detrusorial acontractility
  • urethral strictures
  • neurological bladder
  • not replaceable anticoagulant or antiplatelet drugs for severe cardiological comorbidity
  • bladder cancer;
  • diagnosis or clinical suspicion of prostatic cancer

Sites / Locations

  • University of Bari "Aldo Moro"Recruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Active Comparator

Arm Label

aquablation

holep

pvp

Arm Description

patients with prostatic volume included between 30 and 120 ml will be treated with water jet (aquablation). patients with prostatic volume > 65 ml will be compared with holep arm and patients with prostatic volume included between 30 and 65 ml will be compared with pvp arm.

patients with prostatic volume > 65 ml will be treated with holmium laser technique (Holep)

patients with prostatic volume included between 30 and 65 ml will be treated with photoselective vaporization of prostate (pvp).

Outcomes

Primary Outcome Measures

BOOI variations
non inferiority evaluation of the BOOI variations in patients with LUTS caused by cervico-urethral obstruction by BHP undergone to endoscopic surgery with aquablation versus patients operated with laser endoscopic surgery

Secondary Outcome Measures

IPSS score
Evaluation of the IPSS score variations in two groups of patients,
Qmax
Evaluation of Qmax variations with uroflowmetry and post-voiding residue in two groups;
sexual satisfaction
Evaluation of sexual satisfaction by IIEF-5 survey and evaluation of presence of anejaculation in two groups;

Full Information

First Posted
February 15, 2019
Last Updated
February 18, 2019
Sponsor
University of Bari
Collaborators
Gaetano de Rienzo, Pasquale Ditonno, Francesco Di Modugno, Michele Battaglia, Giuseppe Lucarelli, Marco Spilotros
search

1. Study Identification

Unique Protocol Identification Number
NCT03846700
Brief Title
Urodynamic Evaluation of Disobstrucitve Power of Aquablation VS Laser Techniques
Official Title
Non Inferiority Clinical Randomized Trial Comparing Disobstrucitve Power in Patients With LUTS by BHP (Evaluated With Invasive Advanced Urodynamic Tests) That Underwent to Aquablation, Holep and PVP
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2019 (Anticipated)
Primary Completion Date
October 1, 2019 (Anticipated)
Study Completion Date
December 31, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Bari
Collaborators
Gaetano de Rienzo, Pasquale Ditonno, Francesco Di Modugno, Michele Battaglia, Giuseppe Lucarelli, Marco Spilotros

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
in the last decade, lots of attemps have been done to identify new technologies able to reply the efficacy of gold standard technique for treating BPH, but with a better safety profile. The introduction of laser techniques allowed to reduce complication rates. Among these, considerable importance had Holep and PVP. Aquablation is a recent technique for LUTS treatment. It is minimally invasive, robot-assisted and ultrasound-guided to ablate the prostate in targeted way and in "heat-free" way. It works with high pression water jet. However, in literature informations about disobstructive capacity of minimally invasive techniques, evaluated with invasive urodynamic tests, are low. The enrolled subjects will undergo surgical treatment with one of the techniques under study: Aquablation, HoLEP or PVP. Outpatient visits will be performed at 1, 3 and 6 months after the surgical treatment. During the sixth month visit an invasive urodynamic examination will be performed
Detailed Description
in the last decade, lots of attemps have been done to identify new technologies able to reply the efficacy of gold standard technique for treating BPH, but with a better safety profile. The introduction of laser techniques allowed to reduce complication rates. Among these, considerable importance had Holep and PVP. Aquablation is a recent technique for LUTS treatment. It is minimally invasive, robot-assisted and ultrasound-guided to ablate the prostate in targeted way and in "heat-free" way. It works with high pression water jet. However, in literature informations about disobstructive capacity of minimally invasive techniques, evaluated with invasive urodynamic tests, are low. In particular, about Aquablation, just in one trial is reported the reduction of BOOI, from 49 to 24 in 6 months after surgery, but this information is not associated with standard deviation and statistical significance. Perreira-Carreia, J.A. et al, in 2012 reported a medium BOOI variation after 6 months by surgery, from 60 to 8,7 (p<0,001) even if procedure was conducted with laser 120 W. In 2014 Know, O. and coll., reported BOOI reduction after Holep from 54,9 ± 30,2 to 3,4 ± 17,4 (p<0,001). Actually, there are not trials comparing Aquablation with others mininvasive techniques to treat LUTS by BHP (in particular Holep and PVP). This comparison is very interesting because of the specific benefits of each technique. General and specific aims: non inferiority evaluation of the BOOI variations in patients with LUTS caused by cervico-urethral obstruction by BHP undergone to endoscopic surgery with aquablation versus patients operated with laser endoscopic surgery (primary goal); Evaluation of the IPSS score variations in two groups of patients, Evaluation of Qmax variations with uroflowmetry and post-voiding residue in two groups; Evaluation of sexual satisfaction by IIEF-5 survey and evaluation of presence of anejaculation in two groups; Evaluation of total-PSA variation in two groups; Evaluation of operative times, hospitalization and variations of haemoglobin and haematocrit value in two groups; Evaluation of appearing of side effects (grade 1 and ≥ 2 by Clavien-Dindo) occurred in perioperative period and at 1, 3 and 6 months after surgery; Inclusion criteria: age ≥ 40 years and <90 years; moderate-to-severe lower urinary tract symptoms (IPSS ≥ 12) poor efficacy or tolerance to medical therapy for BPH transrectal ultrasound prostate volume between 30 and 120 ml ability to express written informed consent. Exclusion criteria: previous surgical treatments for BPH indwelling bladder catheter or clean intermittent catheterization bladder stones severe detrusor hypocontractility (BCI <50) or detrusorial acontractility urethral strictures neurological bladder not replaceable anticoagulant or antiplatelet drugs for severe cardiological comorbidity bladder cancer; diagnosis or clinical suspicion of prostatic cancer; Treatment The enrolled subjects will undergo surgical treatment with one of the techniques under study: Aquablation, HoLEP or PVP. The study population will be divided into two cohorts based on prostate volume measured by transrectal ultrasound. Thereafter, patients with a prostate volume between 30 and 65 ml will be assigned to the aquablation arm or PVP arm, while patients with a prostate volume over 65 ml will be subjected to aquablation or HoLEP. The assignment to each of the arms will be randomized, using an on-line software for block randomization. Follow-up: Follow-up visits will be conducted by a blinded research team. Outpatient visits will be performed at 1, 3 and 6 months after the surgical treatment. During the sixth month visit an invasive urodynamic examination will be performed with cystomanometry and pressure-flow study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Benign Prostatic Hyperplasia (BPH)

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
non inferiority, blinded, prospective, randomized clinical trial.
Masking
ParticipantOutcomes Assessor
Masking Description
double blind
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
aquablation
Arm Type
Experimental
Arm Description
patients with prostatic volume included between 30 and 120 ml will be treated with water jet (aquablation). patients with prostatic volume > 65 ml will be compared with holep arm and patients with prostatic volume included between 30 and 65 ml will be compared with pvp arm.
Arm Title
holep
Arm Type
Active Comparator
Arm Description
patients with prostatic volume > 65 ml will be treated with holmium laser technique (Holep)
Arm Title
pvp
Arm Type
Active Comparator
Arm Description
patients with prostatic volume included between 30 and 65 ml will be treated with photoselective vaporization of prostate (pvp).
Intervention Type
Device
Intervention Name(s)
aquablation
Intervention Description
minimally invasive, robot-assisted and ultrasound-guided ablation of the prostate in targeted way and in "heat-free" way working by high pression water jet
Intervention Type
Device
Intervention Name(s)
holep
Intervention Description
holmium laser enucleation of prostate
Intervention Type
Device
Intervention Name(s)
pvp
Intervention Description
photoselectivevaporization of prostate
Primary Outcome Measure Information:
Title
BOOI variations
Description
non inferiority evaluation of the BOOI variations in patients with LUTS caused by cervico-urethral obstruction by BHP undergone to endoscopic surgery with aquablation versus patients operated with laser endoscopic surgery
Time Frame
6 months
Secondary Outcome Measure Information:
Title
IPSS score
Description
Evaluation of the IPSS score variations in two groups of patients,
Time Frame
1, 3 and 6 months
Title
Qmax
Description
Evaluation of Qmax variations with uroflowmetry and post-voiding residue in two groups;
Time Frame
1, 3 and 6 months
Title
sexual satisfaction
Description
Evaluation of sexual satisfaction by IIEF-5 survey and evaluation of presence of anejaculation in two groups;
Time Frame
1, 3 and 6 months
Other Pre-specified Outcome Measures:
Title
PSA
Description
Evaluation of total-PSA variation in two groups
Time Frame
1, 3 and 6 months
Title
complications
Description
Evaluation of appearing of side effects (grade 1 and ≥ 2 by Clavien-Dindo) occurred in perioperative period and at 1, 3 and 6 months after surgery;
Time Frame
1, 3 and 6 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: moderate-to-severe lower urinary tract symptoms (IPSS ≥ 12) poor efficacy or tolerance to medical therapy for BPH transrectal ultrasound prostate volume between 30 and 120 ml ability to express written informed consent. Exclusion Criteria: previous surgical treatments for BPH indwelling bladder catheter or clean intermittent catheterization bladder stones severe detrusor hypocontractility (BCI <50) or detrusorial acontractility urethral strictures neurological bladder not replaceable anticoagulant or antiplatelet drugs for severe cardiological comorbidity bladder cancer; diagnosis or clinical suspicion of prostatic cancer
Facility Information:
Facility Name
University of Bari "Aldo Moro"
City
Bari
ZIP/Postal Code
70124
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Paolo PM Minafra, resident doctor
Phone
3893472729
Ext
0039
Email
minafra.p@gmail.com
First Name & Middle Initial & Last Name & Degree
Francesco FDM Di Modugno, resident doctor
Phone
3315667900
Ext
0039
Email
f.dimodugno1@virgilio.it

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Urodynamic Evaluation of Disobstrucitve Power of Aquablation VS Laser Techniques

We'll reach out to this number within 24 hrs