Trial · NCT02232425
Outcomes13
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 13 of 13
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Mean Fold Change in Geometric Mean Intravaginal Ejaculatory Latency Time (IELT) | Last 4 weeks of treatment compared to baseline | Efficacy data set excluding outliers | No units for fold change | GEOMETRIC_MEAN |
| SECONDARY | Proportion of Participants Rating Their PE as Better or Much Better, on the Clinical Global Impression of Change (CGIC) Scale | Baseline to the end of treatment (approximately 8 weeks) | Intent to treat, excluding outliers | proportion of participants | NUMBER |
| SECONDARY | Proportion of Participants With Greater Than or Equal to (≥) 2.5 Fold Increase in Intravaginal Ejaculatory Latency Time (IELT) | Last 4 weeks of treatment compared to baseline | Intent to treat, excluding outliers | Proportion of participants | NUMBER |
| SECONDARY | Mean Fold Change in Arithmetic IELT (Intravaginal Ejaculatory Latency Time) | Last 4 weeks of treatment compared to baseline | Intent to treat, excluding outliers | No units for fold change | MEAN |
| SECONDARY | Mean Change in Score on Control of Timing of Ejaculation | Last 4 weeks of treatment compared to baseline | Intent to treat, excluding outliers | units on a scale | MEAN |
| SECONDARY | Mean Change in Score on Ejaculation-related Personal Distress | Last 4 weeks of treatment compared to baseline | Intent to treat, excluding outliers | units on a scale | MEAN |
| SECONDARY | Proportion of Participants With ≥ 1 Category of Improvement in Satisfaction With Sexual Intercourse, on the Premature Ejaculation Profile (PEP) Questionnaire | Baseline to 8 weeks | Intent to treat, excluding outliers | adjusted proportion of participants | NUMBER |
| SECONDARY | Proportion of Participants With ≥ 1 Category of Improvement in Control Over Ejaculation During Sexual Intercourse on the Premature Ejaculation Profile (PEP) Questionnaire | Baseline to 8 weeks | Intent to treat, excluding outliers | adjusted proportion of participants | NUMBER |
| SECONDARY | Proportion of Participants With ≥ 1 Category of Improvement in Ejaculation-related Distress on the Premature Ejaculation Profile ( PEP) Questionnaire | Baseline to 8 weeks | Intent to treat, excluding outliers | adjusted proportion of participants | NUMBER |
| SECONDARY | Proportion of Participants With ≥ 1 Category of Improvement in Ejaculation-related Interpersonal Difficulty on the Premature Ejaculation Profile (PEP) Questionnaire | Baseline to 8 weeks | Intent to treat, excluding outliers | adjusted proportion of participants | NUMBER |
| SECONDARY | Proportion of Participants With ≥ 2 Category Increase in Control and ≥ 1 Category Decrease in Personal Distress on a Patient Reported Outcome (PRO) Measure | Baseline to 8 weeks | Intent to treat, excluding outliers | proportion of participants | NUMBER |
| SECONDARY | Change in Percentage of Intercourse Attempts Lasting Longer Than 1 Minute From Baseline to Last 4 Weeks on Treatment | Baseline to last 4 weeks on treatment | Intent to treat, excluding outliers | percentage of attempts | MEAN |
| SECONDARY | Incidence of Treatment-emergent Adverse Events | Start of Treatment to end of study (approximately 10 weeks) | Intent to treat, excluding outliers | participants | NUMBER |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT02232425/outcomes