Selution Sirolimus-eluting Balloon for Internal Pudendal-penile Artery Disease-related Erectile Dysfunction

Study Design

1. Prospective, randomized, single-blinded, two-arm, single-center, first-in-man, proof-of-concept trial.

2. Safety and efficacy measures will be monitored and collected by the study physician/coordinator at hospital discharge, 2 weeks, 1, 3 (12 weeks), 6, and 8 (7-9, study end) months after the index procedure.

3. For patients developing binary restenosis at 12 weeks, angioplasty with Selution SLR drug-eluting balloon (in the drug-eluting balloon [DEB] arm) or plain old balloon (POB)(in the POB arm) will be performed thereafter and secondary patency will be evaluated 5 months later, the originally defined 8-month follow-up.

Target Population

1. Patient profile: Patients with erectile dysfunction according to International Index of Erectile Function-Erectile Function (IIEF-EF) score and distal internal pudendal and/or penile artery stenotic disease identified by pelvic computed tomography angiography (CTA) and confirmed by invasive angiography.

2. Inclusion criteria 2.1 Men ≥20 years of age with erectile dysfunction defined as an IIEF-EF score of ≤25 points; 2.2 The anatomical inclusion criteria, based on pelvic CT angiography, are luminal diameter stenosis of ≥50% in the distal internal pudendal and/or penile arteries with proximal reference vessel diameter of ≥1.5 mm and a target-lesion length of ≤40 mm.

Patients and Sites A total of 54 patients, with at least 54 evaluable lesions, from National Taiwan University Hospital will be enrolled in this trial. 1:2 randomization (18 and 36 in plain old balloon group and Selution group, respectively) will be performed. Pre-specified interim analyses for the primary efficacy outcome measure with an option to prematurely end the study will be conducted while 12, 20, 28, and 36 patients complete evaluation of the primary efficacy measure.

Primary Efficacy Endpoint CT angiographic binary restenosis (≥50% lumen diameter stenosis) at 12 weeks follow-up.

Primary Safety Endpoint The rate of major adverse events at 12 weeks after intervention, defined as procedure-related death, occurrence of perineal hematoma, gangrene or necrosis (glans penis, penile shaft, scrotal, or anal), or the need for subsequent perineal, penile, or anal surgery (including target-lesion or vessel revascularization or arterial embolization procedures).

Secondary Endpoints

1. Invasive angiographic binary restenosis (≥50% lumen diameter stenosis) at 8 (7-9) months follow-up;

2. CT angiographic binary restenosis (≥50% lumen diameter stenosis) at 8 (7-9) months follow-up;

3. Intravascular ultrasound (IVUS)-based binary restenosis (≥50% averaged lumen diameter stenosis) at follow-up;

4. Peak systolic velocity of treated-side cavernosal artery of >35 cm/sec by penile duplex ultrasonography at 12 weeks;

5. Technical success defined as residual diameter stenosis of ≤30% with adequate distal run-off (TIMI 3 flow) by invasive angiography 3 minutes after angioplasty with Selution SLR;

6. Change of IIEF-EF score at 1, 3, 6, and end of follow-up;

7. Clinical success defined as change of IIEF-EF score from baseline by ≥4 points or IIEF-EF ≥26 at 1, 3, 6, and end of follow-up;

8. Clinical worsening defined as decrease in IIEF-EF score from baseline by ≥4 points at 1, 3, 6, and end of follow-up;

9. Changes of invasive angiographic and IVUS parameters, including diameter, diameter stenosis, and late loss between 8 months and baseline;

10. Changes of CT angiographic parameters, including diameter, diameter stenosis, and late loss between 8 months and baseline;

11. Changes of penile duplex ultrasonographic parameters (peak systolic flow, RI) between follow-up and baseline;

12. The rates of major adverse events, defined as procedure-related death, occurrence of perineal hematoma, gangrene or necrosis (glans penis, penile shaft, scrotal, or anal), or the need for subsequent perineal, penile, or anal surgery (including target-lesion or vessel revascularization or arterial embolization procedures), at 1, 3 months, 6 months, and end of follow-up.

Statistical Considerations

1. Sample size estimation: Assuming a binary restenosis rate of 8% with Selution SLR sirolimus-eluting balloon versus a historical restenosis rate of 40% in patients treated with plain old balloon in our PERFECT registry, a minimum of 54 evaluable lesions in 54 patients with a 1:2 randomization ratio (18 and 36 in plain old balloon group and Selution group, respectively) was considered necessary to have a statistical power of 80% and a 2-sided p<0.05 to detect a treatment difference in binary restenosis. Pre-specified interim analyses for the primary efficacy outcome measure with an option to prematurely end the study will be conducted while 12, 20, 28, and 36 patients complete evaluation of the primary efficacy measure.

2. Statistical analysis This prospective, randomized, single-blinded (patient), two-arm, single-center, superiority study is a feasibility trial designed to provide preliminary observations and generate hypotheses for future studies. Continuous variables will be presented as means with standard deviations (SDs). Categorical variables will be presented as counts and percentages. Statistical comparisons between treatment groups will be made using t tests for continuous variables and χ² or Fisher's exact tests for categorical variables. Within each treatment group, paired t tests will be used to compare changes in continuous variables from baseline to follow-up.

Inclusion Criteria

1. Men ≥20 years of age with erectile dysfunction defined as an IIEF-EF score of ≤25 points;

2. The anatomical inclusion criteria, based on pelvic CT angiography, are luminal diameter stenosis of ≥50% in the distal internal pudendal and/or penile arteries with proximal reference vessel diameter of ≥1.5 mm and a target-lesion length of ≤40 mm;

Exclusion Criteria

1. The presence of diameter stenosis of ≥70% in the ipsilateral internal iliac artery, anterior division of internal iliac artery, and/or proximal internal pudendal artery, which could not be successfully treated by angioplasty and stenting;

2. Any non-vascular cause of erectile dysfunction (i.e., pelvic irradiation, pelvic trauma, Peyronie's disease, etc.), which is deemed irreversible by urologist;

3. Untreated hypogonadism (serum total testosterone <2.5 ng/ml) within 28 days before enrollment;

4. Isolated penile veno-occlusive dysfunction (venous leak) by duplex ultrasonography with right or left cavernosal artery end-diastolic velocity >10 cm/s, peak systolic velocity >40 cm/s, and resistance index (RI) <0.75;

5. Acute coronary syndrome, stroke, or life-threatening arrhythmia within 3 months before enrollment;

6. Poorly controlled diabetes mellitus with glycosylated hemoglobin levels >9%;

7. Serum creatinine levels >3.0 mg/dl;

8. Bleeding diathesis precluding the use of antiplatelets or anticoagulants or known hypercoagulopathy;

9. Any malignancy or debilitating disease with life expectancy of fewer than 12 months;

10. Known intolerance to contrast agents, aspirin, heparin, all P2Y12 inhibitors, or sirolimus.

Procedure All patients will be admitted one day prior to the procedure and receive aspirin (100 mg daily) and clopidogrel (75 mg daily and 300 mg loading one day before intervention) 24 h prior to the procedure. Selective angiography and internal pudendal/penile artery interventions will be performed on the second day of hospitalization. All procedures will be done percutaneously by an over-the-bifurcation (for the contralateral lesions) or a retrograde (for the ipsilateral lesions) approach via a single femoral vascular access with the use of a 6-French sheath. The investigators routinely engage the proximal internal pudendal artery by using a 5-French diagnostic/guiding catheter and obtain the selective angiograms following intraarterial administration of 150-200 microg of nitroglycerin to achieve maximal vasodilatation. Use of any phosphodiesterase-5 inhibitor within 72 hours of the procedure will be prohibited.

Patients will proceed with investigational intervention if their quantitative angiographic results fulfilled the following angiographic inclusion criteria: 1) luminal diameter stenosis of ≥50% in the distal internal pudendal and/or penile arteries, 2) a target-lesion proximal reference vessel diameter ≥1.5 mm, and 3) a target-lesion length ≤40 mm. Patients will be excluded if there is ≥70% stenosis in the ipsilateral ilio-pudendal-penile arterial system proximal to the distal internal pudendal artery and not amenable to interventional therapy.

After confirmation of angiographic eligibility, patients will receive 8,000 U of heparin to maintain an activated clotting time ≥250 s. Selective engagement of the internal pudendal artery will be performed with an appropriate-shaped 5-French guiding catheter. A 0.014-inch steerable guidewire will be advanced across the stenosis and IVUS and standard interventional techniques will be applied to the lesion. In order to prevent inadvertent dissection during predilation, the investigators routinely start with a balloon catheter with a diameter ≥0.5 mm smaller than the reference vessel and ended with a balloon catheter with the size approximately equal to the reference vessel diameter. Three minutes after balloon predilation, the investigators will obtain an angiogram. Randomization will take place before angioplasty. If the residual stenosis is ≤30%, no further intervention will be performed in the plain old balloon (POB) group. While in the drug-eluting balloon (DEB) group, the investigators will perform angioplasty with the Selution SLR catheter, inflated at nominal pressure for at least 120 seconds. After dilatation of the entire target-lesion, biplane angiograms and IVUS imaging will be obtained. Technical success is defined as residual diameter stenosis ≤30% and adequate distal run-off. Bail-out stenting will be performed if residual stenosis is >30%, either after plain old balloon angioplasty or angioplasty with Selution SLR. For lesions with residual stenosis >30% but not suitable for stenting, repeat angioplasty will be performed for at most twice.

After intervention, patients will be discharged in the morning of the third day of hospitalization. Post-procedural antiplatelet therapy include aspirin (100 mg daily) indefinitely and clopidogrel (75 mg daily) for a minimum of 3 months.

Patient Follow-up

1. Safety and efficacy measures will be monitored and collected by the study physician/coordinator at hospital discharge, 2 weeks, 1, 3, 6, and 8 (7-9, study end) months after the index procedure. Participants will be encouraged to contact the study physician/coordinator directly by phone whenever the participants feel any discomfort, no matter it is related to the procedure or not.

2. For patients developing binary restenosis at 12 weeks, angioplasty with plain old balloon (in the POB arm) or Selution SLR drug-eluting balloon (in the DEB arm) will be performed thereafter and secondary patency will be evaluated 5 months later, the originally defined 8-month follow-up.

3. For patients developing binary restenosis at 8 months, angioplasty with Selution SLR drug-eluting balloon will be performed. All these patients will be followed for additional 6 months.

Safety Monitoring Safety events including procedure-related death, occurrence of perineal hematoma, gangrene or necrosis (glans penis, penile shaft, scrotal, or anal), or the need for subsequent perineal, penile, or anal surgery (including target-lesion or vessel revascularization or arterial embolization procedures) will be collected by the study physician/coordinator at 1, 3, 6 months, and study end after the index procedure.