Ejaculatory and Orgasmic Dysfunction Registry

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCharitable Union for the Research and Education of Peyronie's Disease

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

None

Trial 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

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

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).

Time frame
3 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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