Cleveland, OHNCT05868668Now EnrollingIRB Ready

Erectile Dysfunction Due to Arterial Insufficiency Clinical Trial in Cleveland, OH

Access cutting-edge erectile dysfunction due to arterial insufficiency treatment through this clinical trial at a research site in Cleveland. Study-provided care at no cost to qualified participants.

Sponsored by The Cleveland Clinic

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Expert Care in Cleveland

Access erectile dysfunction due to arterial insufficiency specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related erectile dysfunction due to arterial insufficiency treatment provided free

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Why Participate?

  • No-Cost Study Care

  • Local to Cleveland

    Convenient for OH residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Cleveland site if eligible
  4. 4Begin participation

About This Erectile Dysfunction Due to Arterial Insufficiency Study in Cleveland

The purpose of this study to perform a randomized, sham controlled analysis of the effectiveness of both fSWT and rWT in the relief of erectile dysfunction and chronic pelvic pain syndrome.

Sponsor: The Cleveland Clinic

Who Can Participate

Inclusion Criteria

(ED): (all of the following)
Cis-gendered heterosexual adult males18 years old
Stable relationship of more than 3 months duration with currently willing sexual partner and desire for penetration.
Mild to moderate organic erectile dysfunction (IIEF-EF score 11-25) in the last 3 months
If ED responsive or partially responsive to current use of PDE5I, participant must be willing to discontinue PDE5I for 4 weeks prior to trial and remain off PDE5I for the duration of the study. Partially responsive ED is defined as inadequate response for desired sexual activity, or poorly maintained erection despite initially good response.
Agreeable to attempt sexual intercourse at least 4 times per month for duration of study without being under the influence of alcohol or recreational drugs
Morning total testosterone level over 300ng/dL

Exclusion Criteria

Nerve-injury related ED (/spinal cord injury, severe lumbosacral disorder (radiculopathy, spinal stenosis) or other neurological disease affecting erectile functions (e.g, multiple sclerosis, alzheimer's disease, parkinsons disease, amyotrophic lateral sclerosis)
Untreated hypogonadism (morning total testosterone \<300 ng/dL) or on androgen deprivation therapy in the last 12 months
Predominately psychogenic ED based upon expert clinician opinion
Peyronie's disease, palpable plaque or curvature/penile anatomic abnormality that affects penetrative intercourse to any degree
History of non-superficial penile surgery (e.g, penile prosthesis, penectomy, plication, grafting)
History of penile injury or trauma (e.g, priapism, penile fracture)
Use of intracavernosal injection for ED within the last year
If diabetic, HbA1c 8% or higher within the past 12 months
Known corporal veno-occlusive dysfunction based on prior Doppler penile ultrasound
Current tobacco smoker, or has smoked in the past year
Poorly controlled hyperlipidemia
Poorly controlled hypertension
Severe cardiac disease or history of myocardial infarction
History of psychiatric disorder including bipolar disorder, current moderate or severe depression
Patients currently using SSRI or psychotropic medication
Severe ED based on IIEF-EF (score 10 or below)
Current acute prostatitis Chronic Pelvic Pain Syndrome Group: Inclusion Criteria (CPPS): (all of the following)
Adult males ≥18 years old
Chronic pelvic pain not explained by concurrent urinary tract infections. urine)
Willing to do PFPT Exclusion criteria (CPPS):
Nerve-injury related pelvic pain (history of /spinal cord injury, severe lumbosacral disorder (radiculopathy, spinal stenosis) or other neurological disease affecting pain in the pelvic region(Multiple sclerosis, Alzheimer's, Parkinsons disease)
Acute prostatitis or any acute infection of the pelvic region
History of pelvic trauma

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Cleveland?

Yes, this clinical trial (NCT05868668) has an active research site in Cleveland, OH that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Erectile Dysfunction Due to Arterial Insufficiency Treatment Options in Cleveland, OH

If you're searching for erectile dysfunction due to arterial insufficiency treatment options in Cleveland, OH, this clinical trial (NCT05868668) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Cleveland research site is actively enrolling participants for this clinical trial. You'll receive care from experienced erectile dysfunction due to arterial insufficiency specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all erectile dysfunction due to arterial insufficiency clinical trials near you to find additional studies recruiting in your area.

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