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Ejaculatory and Orgasmic Dysfunction Registry

Charitable Union for the Research and Education of Peyronie's Disease · NCT06605469

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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

Ejaculatory and Orgasmic Dysfunction Registry (NCT06605469) | Bored Studies