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Clinical Trial Summary

The objectives of this study are to compare the efficacy and safety of Clotrimazole troche/ lozenges USP, 10 mg (Unique Pharmaceutical Laboratories, India) vs. Clotrimazole Troche/ Lozenges USP, 10 mg (Roxane Laboratories Inc., USA) in patients with oropharyngeal candidiasis, where this condition has been diagnosed by clinical examination and confirmed by fungal culture


Clinical Trial Description

This study is Randomized, Double Blind, Parallel, Comparative study. Approximately 26 study sites across India will participate in this study to complete sample size of 360 randomized subjects in order to achieve at least 250 per-protocol (PP) subjects.

Subjects would be assigned randomly to test product or reference product in 1:1 ratio.

Subjects with confirmed oral candidiasis by KOH smear/candidal culture will be given study medication 5 times a day for 14 consecutive days.

The schedule of the subject's visit at study site will be as follows:

1. Visit 1 - Screening visit (-7 Days).

2. Visit 2 - Randomization (Day 1).

3. Visit 3 - Follow Up (Day 8 (+2)).

4. Visit 4 - Follow Up (Day 15 (+2)).

5. Visit 5 - Follow Up/ End of study (Day 21 (+/-4)) Subjects with complete resolution of signs and symptoms of Oral Candidiasis on Day 21 (+/-4) will be considered as treatment success. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02635438
Study type Interventional
Source Thinq Pharma-CRO Pte. Ltd.
Contact Kalpesh B Vispute, Medical
Phone +912225816882
Email kalpesh@thinqcro.com
Status Recruiting
Phase Phase 3
Start date December 2016
Completion date November 2018

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Completed NCT00553137 - Single Dose Versus Two Weeks Course of Fluconazole in the Treatment of Oropharyngeal Candidiasis in HIV Infected Individuals in Tanzania Phase 4