Clinical trial
A Study to Evaluate Intravaginal Ejaculation Time in Men With and Without…
NCT00210678 · Johnson & Johnson Pharmaceutical Research & Development, L.L.C., Industry · Completed
Key facts
| NCT number | NCT00210678 |
|---|---|
| Title | A Study to Evaluate Intravaginal Ejaculation Time in Men With and Without Premature Ejaculation |
| Official title | An Observational Study to Evaluate Intravaginal Ejaculatory Latency Time and Patient-Reported Outcomes in Men With and Without Premature Ejaculation |
| Lead sponsor | Johnson & Johnson Pharmaceutical Research & Development, L.L.C., Industry |
| Status | Completed |
| Study type | Observational |
| Conditions | Erectile Dysfunction |
| Intervention type | Behavioral |
| Interventions | No intervention |
| Enrollment | 1,115 |
| Start date | Mar 1, 2005 |
| Primary completion | Sep 1, 2005 |
| Completion | Sep 1, 2005 |
| First posted | Sep 21, 2005 |
| Last update posted | Oct 10, 2012 |
At a glance
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: