Ejaculatory and Orgasmic Dysfunction Registry
Charitable Union for the Research and Education of Peyronie's Disease · NCT06605469
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Observational
- Target enrollment
- 500
- US sites recruiting
- 1
- Study start
- May 30, 2024
- Record last updated
- August 26, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Conditions: Ejaculatory Dysfunction; Premature Ejaculation; Delayed Ejaculation; Anorgasmia; Anejaculation; Dysejaculation; Dysorgasmia
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
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
Recruiting US locations
The Male Fertility and Peyronie's Clinic
Orem, UT 84057
Site contact: Landon Trost, MD · (888) 655-0015 · email@mfp.clinic
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