Hyannis, MANCT07273773Now EnrollingIRB Ready

Erectile Dysfunction (ED) Clinical Trial in Hyannis, MA

Access cutting-edge erectile dysfunction (ed) treatment through this clinical trial at a research site in Hyannis. Study-provided care at no cost to qualified participants.

Sponsored by Rigicon, Inc.

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Expert Care in Hyannis

Access erectile dysfunction (ed) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related erectile dysfunction (ed) treatment provided free

Apply for This Hyannis Location

Check if you qualify for this erectile dysfunction (ed) clinical trial in Hyannis, MA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Hyannis

    Convenient for MA 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 Hyannis site if eligible
  4. 4Begin participation

About This Erectile Dysfunction (ED) Study in Hyannis

This study evaluates the long-term safety and effectiveness of the Rigicon Infla10® Inflatable Penile Prosthesis in patients with erectile dysfunction. The study follows patients implanted with the Rigicon Infla10® Pulse™ Dynamic Inflatable Penile Prosthesis for up to 3 years after implantation.

Sponsor: Rigicon, Inc.

Who Can Participate

Inclusion Criteria

Male ≥22 years of age.
Diagnosed with erectile dysfunction (impotence).
Agree to receive Infla10® three-piece IPP as an ED treatment.
Willing to complete all protocol required for follow-up visits and tests.

Exclusion Criteria

Contraindication to general anesthesia.
Known allergy or sensitivity to product materials as indicated in the device labeling.
Previous penile prosthesis or prior enlargement surgeries
Diagnosed penile sensory neuropathy.
Patients who are receiving immunosuppressive drugs or have a history of kidney transplantation.
Patients who are receiving chemotherapy at the time of enrolment.
Diagnosed with fibrotic disease, such as priapism or Peyronie's disease or Chordee.
Compromised immune system, such as systemic lupus erythematosus, discoid lupus, or scleroderma.
Uncontrolled diabetes (HbA1c ≥ 9.0% \[≈75 mmol/mol\], measured within 90 days prior to surgery.
Bleeding disorder or coagulopathy that may in the judgment of the investigator preclude safe procedure.
Active urogenital infection or active skin infection in region of surgery or systemic infection at the time of assessment.
Clinically significant comorbidities or presence of unstable conditions (e.g. cardiovascular, lung, renal \[serum creatinine \> 2.0 mg/dl\], hepatic, bleeding disorders, or metabolic impairment) that may confound the results of the study or in the judgment of the physician investigator preclude safe procedure.
Lacking manual dexterity or mental abilities necessary to operate the device.
Expected life expectancy \< two years.
Unwilling or unable to sign the Informed Consent.
Unwilling or unable to comply with the follow-up study requirements.
Psychogenic erectile dysfunction
Currently participating in an investigational drug or another investigational device exemption (IDE) study.
The cognitively challenged subjects and subjects with any cognitive disorder that interferes with or precludes direct and accurate communication with the study investigator regarding the study or affects the ability to complete the study questionnaires.
Incarcerated subjects
Subjects who are currently using, or who have not previously attempted and failed, standard non-surgical ED therapies including oral or topical treatments.

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 Hyannis?

Yes, this clinical trial (NCT07273773) has an active research site in Hyannis, MA 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 (ED) Treatment Options in Hyannis, MA

If you're searching for erectile dysfunction (ed) treatment options in Hyannis, MA, this clinical trial (NCT07273773) 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 Hyannis research site is actively enrolling participants for this clinical trial. You'll receive care from experienced erectile dysfunction (ed) 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 (ed) clinical trials near you to find additional studies recruiting in your area.

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