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Changes in Penile Firmness With Low-Intensity Shockwave Therapy (LiST)

Changes in Penile Firmness With Low-Intensity Shockwave Therapy (LiST)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05756803
Enrollment
20
Registered
2023-03-06
Start date
2022-01-15
Completion date
2025-04-15
Last updated
2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Erectile Dysfunction

Brief summary

Patients presenting with erectile dysfunction are often found to have increased corporal firmness on elastography. We hypothesize that this corporal firmness reflects reversable changes that can be altered by Low-Intensity Shockwave Therapy (LiST). In this pilot study patients found to have increased corporal firmness will be treated with LiST.

Detailed description

This study will enroll men between the ages of 18 and 65 with corporal cavernosal firmness on elastography. The participants study duration is 3 months long and includes eight visits at the study center. Study visits consist of physical exam, vital signs, questionnaires, blood draws, and administration of low-intensity shockware therapy (LiST). Low intensity extracorporeal (i.e., outside the body) shockwave therapy (LiST) is a treatment that has been in use since 2010 and has become commonly used Internationally and in the United States since 2015. The device applies a low-intensity shockwave to the surface of the penis using an ultrasound gel as the coupling agent. The study will evaluate changes in corporal cavernosal firmness and changes in penile vascular blood flow.

Interventions

DEVICELow-intensity acoustic shockwave therapy

The study is being done to find out if low-intensity shockwave therapy can improve penile blood flow and restore sexual function in men with impaired erectile function.

Sponsors

Northwell Health
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 64 Years
Healthy volunteers
Yes

Inclusion criteria

1. Provision of signed and dated informed consent form 2. Stated willingness to comply with all study procedures and availability for the duration of the study 3. Men aged 18-64 4. Sexually active men and evidence of increased firmness on elastography during their standard evaluation for erectile dysfunction.

Exclusion criteria

1. Within two weeks of Visit 1 using erectogenic medications including PDE5 inhibitors and/or penile injection therapy 2. Presence of a penile implant. 3. Presence of cardiac pacemaker or defibrillator 4. Patients who are using devices which are sensitive to electromagnetic radiation. 5. Screening ultrasound positive for testicular cancer 6. Presence of untreated prostate cancer 7. Patients with severe coagulation disorders 8. Patient that in the opinion of the Principal Investigator would be non-compliant with the study

Design outcomes

Primary

MeasureTime frameDescription
Evaluate changes in corporal cavernosal firmness with Low-Intensity Acoustic Shockwave Therapy (LiST)12 WeeksChange in corporal firmness (KPa) with Low-Intensity Acoustic Shockwave Therapy (LiST)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026