Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
500 participants
OBSERVATIONAL
2024-05-30
2029-05-31
Brief Summary
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Participants will submit questionnaires about their diagnosis and treatment efficacy and multiple time intervals.
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Detailed Description
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Subjects meeting criteria will be offered study entry by their local provider who will refer them to an email address to indicate their interest. Participants will then be administered questionnaires at baseline and every 3 months x 1 year, followed by every 6 months x 2 years. Patient partners will also be allowed to enroll and will receive questionnaires on the same schedule (baseline, q3 months x 1 year, q6 months x 2 years).
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* For partners, inclusion is being a sexual partner of a man with ejaculatory and/or orgasmic dysfunction who is receiving treatment
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
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Charitable Union for the Research and Education of Peyronie's Disease
OTHER
Responsible Party
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Locations
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The Male Fertility and Peyronie's Clinic
Orem, Utah, United States
Countries
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Facility Contacts
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Other Identifiers
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CUREPD200
Identifier Type: -
Identifier Source: org_study_id
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