Imaging and Interventional Study for Erectile Dysfunction and Lower Urinary Tract Symptoms (PERFECT)
Primary Purpose
Erectile Dysfunction, Lower Urinary Tract Symptoms, Peripheral Arterial Disease
Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
drug-eluting balloon
biodegradable vascular scaffold stent
Apex™ PTCA Dilatation Catheter
Stent System
Sponsored by
About this trial
This is an interventional treatment trial for Erectile Dysfunction focused on measuring Erectile dysfunction, Lower Urinary Tract Symptoms, Peripheral Arterial Disease, Angioplasty, Multidetector Computed Tomography
Eligibility Criteria
Inclusion Criteria:
- men 20 years of age or older with "consistent" erectile dysfunction defined as both IIEF-5 scores, taken at least 4 weeks apart, are in the range of 5 to 21 points and with a difference of <=2 points
- the anatomical inclusion criteria, based on pelvic CT angiography, are unilateral luminal diameter stenosis >=70% or bilateral diameter stenoses >=50% in the pelvic arteries with reference vessel diameter >=2.5 mm and <=4.0 mm and a target-lesion length <=40 mm
Exclusion Criteria:
- the arterial inflow to the penis is entirely from the accessory pudendal arteries rather than the usual internal pudendal artery and common penile artery;
- the presence of focal diameter stenosis >=70% in the common iliac artery, internal iliac artery, or anterior division of internal iliac artery;
- previous radical prostatectomy, pelvic radiation, or Peyronie's disease;
- untreated hypogonadism (serum total testosterone <300 ng/dL within 14 days before enrollment);
- acute coronary syndrome, stroke, or life-threatening arrhythmia within 3 months before enrollment;
- poorly controlled diabetes mellitus with glycosylated hemoglobin levels >9%;
- serum creatinine levels >2.5 mg/dL;
- bleeding diathesis or known hypercoagulopathy;
- life expectancy of fewer than 12 months;
- known intolerance to contrast agents
Sites / Locations
- National Taiwan University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Active Comparator
Active Comparator
Active Comparator
Active Comparator
Arm Label
Angioplasty alone
Stenting
drug-eluting balloon
biodegradable vascular scaffold stent
Arm Description
plain old balloon angioplasty alone
Balloon angioplasty plus stenting
Balloon angioplasty with drug-eluting balloon
Stenting with biodegradable vascular scaffold stent
Outcomes
Primary Outcome Measures
IIEF
IIEF: Internal index for erectile function
EPS
EPS: erectile hardness score
IPSS
IPSS: international prostate symptom score
Secondary Outcome Measures
CT angiographic binary restenosis
CT angiographic binary restenosis: ≥50% lumen diameter stenosis
Full Information
NCT ID
NCT02178761
First Posted
June 22, 2014
Last Updated
June 30, 2014
Sponsor
National Taiwan University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02178761
Brief Title
Imaging and Interventional Study for Erectile Dysfunction and Lower Urinary Tract Symptoms
Acronym
PERFECT
Official Title
Comprehensive Imaging and Interventional Therapy Studies for Arteriogenic Erectile Dysfunction and Lower Urinary Tract Symptoms: A Multi-modality, Multi-Specialty Collaborative Study (PERFECT Program)
Study Type
Interventional
2. Study Status
Record Verification Date
June 2014
Overall Recruitment Status
Unknown status
Study Start Date
October 2012 (undefined)
Primary Completion Date
June 2016 (Anticipated)
Study Completion Date
June 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Erectile dysfunction is highly prevalent as men grow older. Among the various causes of erectile dysfunction, it has been shown that pelvic arterial insufficiency plays a very important role. The investigators have recently developed the first imaging analytical algorithm by using the abdominal/pelvis multidetector computed tomographic (MDCT) angiography to delineate the whole arterial system supplying the penis. To establish a comprehensive, cutting-edge diagnostic and interventional therapeutic program for erectile dysfunction, the investigators therefore design this series of studies by including experts from Urology, Radiology, and Cardiology. This research project (PERFECT program) includes the following 4 sub-studies: 1) differential frequency of obstructive pelvic arterial lesions in coronary artery disease patients with and without erectile dysfunction/lower urinary tract symptoms (LUTS), 2) differential frequency of obstructive pelvic arterial lesions in patients with vascular risk factors and with or without erectile dysfunction/LUTS, 3) safety, feasibility, and efficacy of comprehensive pelvic angioplasty (with various interventional strategies/instruments) for patients with erectile dysfunction/LUTS and pelvic obstructive arterial disease: proof-of-concept study; and 4) efficacy and safety of comprehensive pelvic angioplasty (with various interventional strategies/instruments) for patients with erectile dysfunction/LUTS and pelvic obstructive arterial disease: a randomized controlled trial.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Erectile Dysfunction, Lower Urinary Tract Symptoms, Peripheral Arterial Disease
Keywords
Erectile dysfunction, Lower Urinary Tract Symptoms, Peripheral Arterial Disease, Angioplasty, Multidetector Computed Tomography
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Angioplasty alone
Arm Type
Active Comparator
Arm Description
plain old balloon angioplasty alone
Arm Title
Stenting
Arm Type
Active Comparator
Arm Description
Balloon angioplasty plus stenting
Arm Title
drug-eluting balloon
Arm Type
Active Comparator
Arm Description
Balloon angioplasty with drug-eluting balloon
Arm Title
biodegradable vascular scaffold stent
Arm Type
Active Comparator
Arm Description
Stenting with biodegradable vascular scaffold stent
Intervention Type
Device
Intervention Name(s)
drug-eluting balloon
Other Intervention Name(s)
SeQuent® Please
Intervention Description
angioplasty completed with drug-eluting balloons
Intervention Type
Device
Intervention Name(s)
biodegradable vascular scaffold stent
Other Intervention Name(s)
Absorb Bioresorbable Vascular Scaffold System
Intervention Description
Stenting with biodegradable vascular scaffold stents
Intervention Type
Device
Intervention Name(s)
Apex™ PTCA Dilatation Catheter
Other Intervention Name(s)
TREK & MINI TREK Coronary Dilatation Catheter, Sprinter Legend RX
Intervention Description
plain old balloon angioplasty alone
Intervention Type
Device
Intervention Name(s)
Stent System
Other Intervention Name(s)
Promus PREMIER™ Everolimus-Eluting Platinum Chromium Coronary Stent System, XIENCE PRIME Everolimus Eluting Coronary Stent System, Resolute Integrity Coronary Stent System, BioMatrix Flex™, Nobori® Drug Eluting Stent, MULTI-LINK 8 Coronary Stent System, Integrity Coronary Stent System
Intervention Description
stenting with either bare-metal stents or drug-eluting stents
Primary Outcome Measure Information:
Title
IIEF
Description
IIEF: Internal index for erectile function
Time Frame
1 year
Title
EPS
Description
EPS: erectile hardness score
Time Frame
1 year
Title
IPSS
Description
IPSS: international prostate symptom score
Time Frame
1 year
Secondary Outcome Measure Information:
Title
CT angiographic binary restenosis
Description
CT angiographic binary restenosis: ≥50% lumen diameter stenosis
Time Frame
1 year
Other Pre-specified Outcome Measures:
Title
Any major adverse events
Time Frame
1year
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
men 20 years of age or older with "consistent" erectile dysfunction defined as both IIEF-5 scores, taken at least 4 weeks apart, are in the range of 5 to 21 points and with a difference of <=2 points
the anatomical inclusion criteria, based on pelvic CT angiography, are unilateral luminal diameter stenosis >=70% or bilateral diameter stenoses >=50% in the pelvic arteries with reference vessel diameter >=2.5 mm and <=4.0 mm and a target-lesion length <=40 mm
Exclusion Criteria:
the arterial inflow to the penis is entirely from the accessory pudendal arteries rather than the usual internal pudendal artery and common penile artery;
the presence of focal diameter stenosis >=70% in the common iliac artery, internal iliac artery, or anterior division of internal iliac artery;
previous radical prostatectomy, pelvic radiation, or Peyronie's disease;
untreated hypogonadism (serum total testosterone <300 ng/dL within 14 days before enrollment);
acute coronary syndrome, stroke, or life-threatening arrhythmia within 3 months before enrollment;
poorly controlled diabetes mellitus with glycosylated hemoglobin levels >9%;
serum creatinine levels >2.5 mg/dL;
bleeding diathesis or known hypercoagulopathy;
life expectancy of fewer than 12 months;
known intolerance to contrast agents
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tzung-Dau Wang, MD, PhD
Phone
+886-972651070
Email
tdwang@ntu.edu.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tzung-Dau Wang, MD, PhD
Organizational Affiliation
NTUH
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Taiwan University Hospital
City
Taipei City
ZIP/Postal Code
10002
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tzung-Dau Wang, MD, PhD
Phone
+886-972651070
Email
tdwang@ntu.edu.tw
First Name & Middle Initial & Last Name & Degree
Tzung-Dau Wang, MD, PhD
First Name & Middle Initial & Last Name & Degree
Wen-Jeng Lee, MD, PhD
12. IPD Sharing Statement
Citations:
PubMed Identifier
24832642
Citation
Wang TD, Lee WJ, Yang SC, Lin PC, Tai HC, Hsieh JT, Liu SP, Huang CH, Chen WJ, Chen MF. Safety and six-month durability of angioplasty for isolated penile artery stenoses in patients with erectile dysfunction: a first-in-man study. EuroIntervention. 2014 May;10(1):147-56. doi: 10.4244/EIJV10I1A23.
Results Reference
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Imaging and Interventional Study for Erectile Dysfunction and Lower Urinary Tract Symptoms
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