Efficacy and Safety Evaluating Fispemifene in the Treatment of Hypogonadal Men With Erectile Dysfunction Unresponsive to PDE5 Inhibitors - NCT00415571-08690 (Clinical Trial 159458)
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Hamilton |
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NJ |
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08690 |
| 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 |
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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Clinical trials are medical research studies designed to test the safety and/or
effectiveness of new drugs, devices, or treatments in humans. These studies are
conducted worldwide for a range of conditions and illnesses. Learn more about
clinical research and participating in a study at
About Clinical Trials.
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