Ejaculatory and Orgasmic Dysfunction Registry

NCT06605469 | Recruiting

• 1 other identifier: CUREPD200
• Study Type: observational
• Target: 500
• Locations: 1 country
• Sites: 1

Brief 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.

Conditions

Ejaculatory Dysfunction; Premature Ejaculation; Delayed Ejaculation; Anorgasmia; Anejaculation; Dysejaculation; Dysorgasmia

Keywords

ejaculatory dysfunction; premature ejaculation; delayed ejaculation; anorgasmia; anejaculation; dysejaculation; dysorgasmia

Outcome Measures

Primary Outcomes (1)

• Primary Objective

  Report subjective efficacy of therapies used to treat ejaculatory dysfunction. Study participants will have the option of indicating if they had used any treatments to treat ejaculatory disorders. If so, they will then be asked to measure its efficacy at improving their symptoms using a 1-10 scale (10 being very effective).

  3 years

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Adult men (\>18) diagnosed with ejaculatory and/or orgasmic dysfunction who were recommended to begin any treatment for the condition For partners, inclusion is being a sexual partner of a man with ejaculatory and/or orgasmic dysfunction who is receiving treatment

You may qualify if:

• Men being treated for either ejaculatory and/or orgasmic dysfunction

You may not qualify if:

• None

Sponsors & Collaborators

• Charitable Union for the Research and Education of Peyronie's Disease: lead

Study Sites (1)

The Male Fertility and Peyronie's Clinic

Orem, Utah, 84057, United States

RECRUITING

MeSH Terms

Conditions

Ejaculatory Dysfunction; Premature Ejaculation

Condition Hierarchy (Ancestors)

Genital Diseases, Male; Genital Diseases; Urogenital Diseases; Sexual Dysfunction, Physiological; Male Urogenital Diseases; Sexual Dysfunctions, Psychological; Mental Disorders

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Target Duration: 3 Years
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 13, 2024
• First Posted: September 20, 2024
• Study Start: May 30, 2024
• Primary Completion (Estimated): May 31, 2029
• Study Completion (Estimated): May 31, 2029
• Last Updated: February 14, 2025

Record last verified: 2025-02

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)