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Last Updated: July 1, 2022

CLINICAL TRIALS PROFILE FOR MICONAZOLE NITRATE COMBINATION PACK


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All Clinical Trials for Miconazole Nitrate Combination Pack

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00194324 ↗ Effect of Exercise on Spread of the Miconozole Nitrate OVULE in the Vagina Completed Johnson & Johnson Phase 4 2004-07-01 This study uses MRI to detect the spread of the Miconozole Nitrate OVULE within the vagina. The effect of moderate amounts of physical activity on the spread will be evaluated, and compared to no physical activity.
NCT00194324 ↗ Effect of Exercise on Spread of the Miconozole Nitrate OVULE in the Vagina Completed University of Pennsylvania Phase 4 2004-07-01 This study uses MRI to detect the spread of the Miconozole Nitrate OVULE within the vagina. The effect of moderate amounts of physical activity on the spread will be evaluated, and compared to no physical activity.
NCT00498680 ↗ Safety and Clinical Effectiveness of 2 Lower Dose Combined PDE5i's vs. Single Maximal Dose PDE5i Unknown status Rambam Health Care Campus Phase 4 2007-03-01 A prospective, randomized, 3-arm parallel trial on 45 males with ED that were never exposed to PDE5i therapy (naïve patients) will be enrolled.In each group, every patient will receive three treatment regimes (Viagra®50mg & Levitra®10mg, Viagra®100mg, Levitra®20mg), in different sequences of administration in such a manner that eventually each patient will receive all regimes in a double- blinded fasion.Safety will be evaluated at pre- screening by measuring hourly vital signs (blood pressure, heart rate)for 4 consecutive hours after taking half-dose combination. Any decrease in blood pressure of 20 mmhg below baseline will exclude the subject from the study. Effcacy will be evaluated by questionnaires (IIEF, Quality of erection questionnaire, grade of erection scale, Sear, QVS and Sexual Encounter Profiles for each sexual event). Non-parametric statistical analysis of the collected data Comparing the 3 groups will be performed.
NCT00702507 ↗ Prospective Two-Year Study to Assess Miconazole Nitrate Resistance in Neonates and Infants Completed GlaxoSmithKline Phase 4 2007-05-01 The purpose of this study is to determine whether repeated use of 0.25% miconazole nitrate ointment in newborns and infants with a yeast infection in the diaper area causes the yeast to become resistant to the drug.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Miconazole Nitrate Combination Pack

Condition Name

Condition Name for Miconazole Nitrate Combination Pack
Intervention Trials
Vulvovaginal Candidiasis 2
Antifungal Drug Adverse Reaction 1
Diaper Rash 1
Health 1
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Condition MeSH

Condition MeSH for Miconazole Nitrate Combination Pack
Intervention Trials
Candidiasis, Vulvovaginal 2
Candidiasis 2
Tinea cruris 1
Tinea 1
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Clinical Trial Locations for Miconazole Nitrate Combination Pack

Trials by Country

Trials by Country for Miconazole Nitrate Combination Pack
Location Trials
United States 6
Ecuador 1
Brazil 1
Dominican Republic 1
Belgium 1
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Trials by US State

Trials by US State for Miconazole Nitrate Combination Pack
Location Trials
Missouri 1
Texas 1
Georgia 1
Florida 1
California 1
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Clinical Trial Progress for Miconazole Nitrate Combination Pack

Clinical Trial Phase

Clinical Trial Phase for Miconazole Nitrate Combination Pack
Clinical Trial Phase Trials
Phase 4 3
Phase 2 2
Phase 1 2
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Clinical Trial Status

Clinical Trial Status for Miconazole Nitrate Combination Pack
Clinical Trial Phase Trials
Completed 5
Not yet recruiting 1
Unknown status 1
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Clinical Trial Sponsors for Miconazole Nitrate Combination Pack

Sponsor Name

Sponsor Name for Miconazole Nitrate Combination Pack
Sponsor Trials
Aesculape CRO Belgium BV 1
Johnson & Johnson 1
University of Pennsylvania 1
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Sponsor Type

Sponsor Type for Miconazole Nitrate Combination Pack
Sponsor Trials
Industry 6
Other 4
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