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Ejaculatory and Orgasmic Dysfunction Registry

NCT06605469 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2025-02-14

No results posted yet for this study

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

Sponsors & Collaborators

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

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-05-30
Primary Completion
2029-05-31
Completion
2029-05-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06605469 on ClinicalTrials.gov