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Capacity problems
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Extra Corporal Shock wave Therapy Has proven effective as treatment with mild to moderate erectile dysfunction in men with erectile dysfunction. Investigator will examine whether the treatment also applies to men with moderate to severe erectile dysfunction after nerve injury associated with prostatectomy.
All patients have undergone prostatectomy and are without recurrence. None of the men have sufficient effect of medical treatment for erectile dysfunction (tablets or injection therapy).
Each participant will fill out two validated sexual function questionnaires: IIEF-5 (International Index of Erectile Function), and EHS (Erection Hardness Score).
Our treatment protocol consists of one treatment sessions per week for 5 wk. The shockwaves are delivered to the distal, mid, and proximal penile shaft, and the left and right crura. The duration of each LI-ESWT session was about 20min, and each session comprised 500 shocks per treatment point (3000 per session) at an energy density of 0.15 mJ/mm2.
Patients are randomized to active treatment or placebo.By placebo added a blocking membrane in the machine, handling is carried out exactly the same way as the active treatment. None of the attending staff members will be familiar with who receive active and who receive placebo treatment.
For evaluation, the International index of erectile function (IIEF-5) will be used after 1, 3- and 6-mo follow-up.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| ESWT | Active Comparator | 500 shockwave 3 different points on penis bilateral |
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| Placebo | Placebo Comparator | 500 shockwave 3 different points on penis bilateral |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Extracorporeal Shockwave Terapy | Procedure | Intervention is treatment with ESWT. Placebo treatment is using the same device as the active treatment, but the shock waves stopped in a non pressure-conductive filter |
| Measure | Description | Time Frame |
|---|---|---|
| IIEF-5 point | Change in IIEF-5 point | 1, 3 and 6 months |
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Inclusion Criteria:
Exclusion Criteria:
Only humans with a penis
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| OUH | Odense | 5000 | Denmark |
All results will be published
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Randomization to active or placebo treatment.
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Patient and therapist are blind. Primary investigator is not blind. Unblinding occurs 3 months after the end of treatment
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