View Clinical Trial (Medical Research Study)
Efficacy and Safety Evaluating Fispemifene in the Treatment of Hypogonadal Men With Erectile Dysfunction Unresponsive to PDE5 Inhibitors - NCT00415571-71913(Clinical Trial 159452)
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Hot Springs |
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State:
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AR |
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71913 |
| Conditions: |
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Hypogonadism - Erectile Dysfunction |
| Purpose: |
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The objective of the study is to assess and compare the preliminary efficacy, safety and
tolerability of fispemifene 300 mg and placebo given once daily for 8 weeks in the treatment
of hypogonadal men with erectile dysfunction (ED) unresponsive to PDE5 inhibitors.
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
- Hypogonadal (morning total testosterone levels ≤400 ng/dl) men age ≥20 with ED who
are unresponsive to PDE5 inhibitors, as demonstrated by International Index of
Erectile Function (IIEF) results for 28-day lead in period. |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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February 1, 2010 |
Modifications to
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