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Clinical Research Detail |
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Title Of Study |
An exploratory, double blind, randomized, parallel group, placebo controlled, multicentric study to evaluate the efficacy and safety of ProvestraTM in female sexual dysfunction (FSD).
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Disease Condition |
Female with sexual dysfunction
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Phase of Trial |
Phase-2
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Discipline |
Pharmacology
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Start date of Trial |
1/17/2011
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Closing Date of Trial |
4/17/2011
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