Ejaculatory and Orgasmic Dysfunction Registry
The goal of this observational study is to evaluate the safety and efficacy of various therapies used to treat ejaculatory and/or orgasmic dysfunctions in men. The objective is to create a large, national registry designed to capture key outcomes for men being treated for ejaculatory and/or orgasmic dysfunction. Partic
| Condition(s) | Ejaculatory Dysfunction, Premature Ejaculation, Delayed Ejaculation, Anorgasmia, Anejaculation, Dysejaculation, Dysorgasmia |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | The goal of this observational study is to evaluate the safety and efficacy of various therapies used to treat ejaculatory and/or orgasmic dysfunctions in men. The objective is to create a large, national registry designed to capture key outcomes for men being treated for ejaculatory and/or orgasmic dysfunction. Participants will submit questionnaires about their diagnosis and treatment efficacy and multiple time intervals. |
| Who can participate | Inclusion Criteria: * Men being treated for either ejaculatory and/or orgasmic dysfunction * For partners, inclusion is being a sexual partner of a man with ejaculatory and/or orgasmic dysfunction who is receiving treatment Exclusion Criteria: * None |
| Ages | 18 Years |
| Sex | All |
| Accepts healthy volunteers | Yes |
| Lead sponsor | Charitable Union for the Research and Education of Peyronie's Disease |
| Locations | Orem, Utah, United States |
| Start date | 2024-05-30 |
| NCT ID | NCT06605469 |
| Official listing | https://clinicaltrials.gov/study/NCT06605469 |