Learn more about the United Clinical Study for Infla10® Pulse™ Dynamic Inflatable Penile Prosthesis (DIPP). Complete the form below. A study team member may contact you to share general study information about eligibility, study procedures, and participation.
Learn more about the United Clinical Study for Infla10® Pulse™ Dynamic Inflatable Penile Prosthesis (DIPP). Complete the form below. A study team member may contact you to share general study information about eligibility, study procedures, and participation.
Thank you for your interest in the Infla10® Pulse™ clinical study. By completing the form below, you can request detailed information about the study, eligibility criteria, and what participation involves.
After you submit this form, a member of our study team will contact you using your preferred method (email or phone) to provide information about the clinical study and answer your questions.
Requesting information does not obligate you to participate in the study. You are free to ask questions, learn about the study, and make an informed decision about whether participation is right for you.
Please Note: Contacting us does not guarantee eligibility or enrollment in the clinical study. Final eligibility is determined by the study team through a comprehensive medical evaluation based on specific inclusion and exclusion criteria.
Please complete the form below to request information about the clinical study. All fields marked with an asterisk (*) are required.
"*" indicates required fields
Privacy Notice: Rigicon takes your privacy very seriously. We will never sell your contact information to any third party. We take steps to protect your information and handle it in accordance with HIPAA, IRB requirements, and applicable laws.
After you submit your request for information, here's what you can expect from our study team.
We will make reasonable efforts to respond within 1–2 business days using your preferred contact method (email or phone).
You will receive detailed information about the clinical study, including eligibility criteria, study procedures, time commitment, and what participation involves.
Our study team will answer your questions about the study and help you understand what participation would involve for your specific situation.
If you are interested in learning more after receiving initial information, the study team will guide you through the screening and evaluation process.
Requesting information and speaking with the study team does not obligate you to participate in the clinical study. You are free to ask questions, learn about the study, and make an informed decision. Participation is completely voluntary.
You can also contact a participating site directly to learn more about the clinical study and discuss potential eligibility with a study coordinator.
Contacting a site does not guarantee eligibility or enrollment in the clinical study.
2805 Veterans Memorial Hwy STE 5
Ronkonkoma, NY 11779
USA
This website is a patient information resource owned by Rigicon, Inc. for educational purposes about the Infla10® Pulse™ clinical study.
Investigational Device. Limited by Federal (or United States) law to investigational use. The Infla10® Pulse™ device is investigational and is being evaluated for safety and performance effectiveness in clinical studies. This website provides educational information only and does not constitute medical advice. This is not advertising and does not offer the device for sale. Participation in the clinical study is voluntary and eligibility is determined by the study team based on specific medical criteria. Not all individuals will qualify. Submitting this form does not guarantee eligibility or enrollment. Please consult with your healthcare provider for personalized medical guidance.
I hereby provide my express consent to be contacted by Rigicon and/or authorized representatives of the participating clinical study sites regarding the UNITED Clinical Study. I agree that the contact information I provide (including phone and email) may be used for screening purposes and to provide information about the study steps.
I understand and agree that:
Rigicon is committed to protecting the privacy and confidentiality of your personal and health-related information. By submitting this form, you acknowledge that the information provided is for the sole purpose of evaluating your potential eligibility for the UNITED Clinical Study.
Please be advised that: