Ultrasound-Guided Photoselective Vaporization of the Prostate
Primary Purpose
Benign Prostatic Hyperplasia
Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Transrectal Ultrasound
Sponsored by
About this trial
This is an interventional treatment trial for Benign Prostatic Hyperplasia focused on measuring Benign Prostatic Hyperplasia, Lower urinary tract symptoms, Photoselective laser vaporization of the prostate, Transrectal Ultrasound
Eligibility Criteria
Inclusion Criteria:
- patients between the ages of 40 and 85
- patients with BPH
- patients scheduled for PVP
Exclusion Criteria:
- patients with known prostate cancer
- patients with bleeding problems
- patients with previous rectal surgery
- patients with anal stenosis
- patients who cannot tolerate anesthesia or in whom anesthesia is considered high-risk
- patients with previous pelvic irradiation
- patients with penile implants
- patients with artificial urinary or rectal sphincters
- patients who are unwilling or unable to sign informed consent
Sites / Locations
- Johns Hopkins Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Transrectal ultrasound
Arm Description
TRUS and TRUS-Robot will be used during PVP
Outcomes
Primary Outcome Measures
Measurement of prostate volume.
Prostate volume will be measured before (Set I, initial: 3 min) and after (Set F, final: 3 min) the PVP.
Measurement of the prostate cavity.
Measurement will be estimated from the 3-D ultrasound Set F.
Recording patient-completed questionnaires (International Prostate Symptom Score (IPSS).
Secondary Outcome Measures
Measurement of complications from the procedure including rectal injury.
Full Information
NCT ID
NCT02346500
First Posted
October 28, 2013
Last Updated
September 14, 2018
Sponsor
Johns Hopkins University
1. Study Identification
Unique Protocol Identification Number
NCT02346500
Brief Title
Ultrasound-Guided Photoselective Vaporization of the Prostate
Official Title
Ultrasound-Guided Photoselective Vaporization of the Prostate
Study Type
Interventional
2. Study Status
Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
December 2012 (Actual)
Primary Completion Date
November 26, 2016 (Actual)
Study Completion Date
November 26, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Benign prostatic hyperplasia (BPH) is a major cause of lower urinary tract symptoms (LUTS) affecting aging men. Medical therapy for BPH includes alpha adrenergic blockers and 5α-reductase inhibitors. In men with moderate-severe LUTS due to BPH, surgical therapy should be considered for 1) those who failed medical therapy and/or 2) those with refractory urinary retention, renal insufficiency secondary to BPH, recurrent urinary tract infections (UTI's), or bladder stones. The gold standard for the surgical therapy of BPH has been transurethral resection of the prostate (TURP). However, TURP is associated with significant comorbidities such as bleeding, prolonged catheterization, and absorptional hyponatremia. To minimize these problems associate with TURP, alternative minimally invasive treatment techniques have been developed. Two of the most commonly used treatment modalities include a photoselective laser vaporization of the prostate (GreenLight PVP) using the potassium titanyl phosphate (KTP) laser and holmium laser enucleation of prostate (HoLEP). The major problem in all these minimally invasive treatment modalities is that they are generally associated with a higher retreatment rate. In addition, there is no intraoperative and objective measurement, other than a limited, transurethral visualization of the prostatic cavity, to assess the extent of the vaporization or enucleation.
We propose to use the transrectal ultrasound (TRUS) and a novel robot, the TRUS robot, to hold and manipulate the TRUS probe to monitor the extent of the vaporization or enucleation of the prostate gland intraoperatively. TRUS has been extensively used for the biopsy needle guidance during prostate biopsy. However, it has never been used during transurethral prostate procedure. The TRUS Robot has been used safely in the current clinical trial, NA_00027540, Ultrasound-Guided Navigation in Robot-Assisted Laparoscopic Radical Prostatectomy. We would like to study the feasibility and safety of using TRUS and the TRUS Robot to monitor the minimally invasive treatment of BPH, such as GreenLight PVP.
Detailed Description
In the current pilot safety and feasibility (S&F) study for ultrasound-guided PVP (UG-PVP), we propose to use TRUS and the TRUS-Robot to record ultrasound images during PVP in 10 patients. The PVP procedure will be conducted as usual, without using the ultrasound for guiding the intervention. TRUS images of the prostate gland and the intraprostatic cavity formed during the PVP procedure will be recorded. These will include three dimensional (3-D) images acquired at the beginning and end of the operation. In addition, real-time 2-D images will be recorded during the case. Recorded images will then be analyzed offline to observe the extent of the vaporization or enucleation of the prostate gland.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Benign Prostatic Hyperplasia
Keywords
Benign Prostatic Hyperplasia, Lower urinary tract symptoms, Photoselective laser vaporization of the prostate, Transrectal Ultrasound
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
1 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Transrectal ultrasound
Arm Type
Experimental
Arm Description
TRUS and TRUS-Robot will be used during PVP
Intervention Type
Device
Intervention Name(s)
Transrectal Ultrasound
Intervention Description
The TRUS and TRUS-Robot will be used to record ultrasound images during PVP. The PVP procedure will be conducted as usual, without using the ultrasound for guiding the intervention.
Primary Outcome Measure Information:
Title
Measurement of prostate volume.
Description
Prostate volume will be measured before (Set I, initial: 3 min) and after (Set F, final: 3 min) the PVP.
Time Frame
During the study procedure, after the TRUS probe is in position for imaging of the prostate.
Title
Measurement of the prostate cavity.
Description
Measurement will be estimated from the 3-D ultrasound Set F.
Time Frame
At the end of the PVP procedure.
Title
Recording patient-completed questionnaires (International Prostate Symptom Score (IPSS).
Time Frame
Measurements will be recorded 3 months after the PVP procedure.
Secondary Outcome Measure Information:
Title
Measurement of complications from the procedure including rectal injury.
Time Frame
Measurements will be recorded during the PVP procedure.
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients between the ages of 40 and 85
patients with BPH
patients scheduled for PVP
Exclusion Criteria:
patients with known prostate cancer
patients with bleeding problems
patients with previous rectal surgery
patients with anal stenosis
patients who cannot tolerate anesthesia or in whom anesthesia is considered high-risk
patients with previous pelvic irradiation
patients with penile implants
patients with artificial urinary or rectal sphincters
patients who are unwilling or unable to sign informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Misop Han, M.D., M.S.
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins Hospital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Ultrasound-Guided Photoselective Vaporization of the Prostate
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