Search for Clinical Trial Results

Candidiasis - 83 Studies Found
Status | Study |
Completed |
Study Name: Safety and Immunogenicity Study of a Virosomal Vaccine Against Recurrent Vulvovaginal Candida Infection Condition: Recurrent Vulvovaginal Candidiasis Date: 2010-02-10 Interventions:
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Completed |
Study Name: Arasertaconazole Nitrate Pessaries - Dose Finding Study for the Vulvovaginal Candidiasis (VVC) Treatment Condition: Vulvovaginal Candidiasis Date: 2010-06-09 Interventions:
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Completed |
Study Name: A Randomized Study Evaluating the Therapeutic Equivalence of Two Butoconazole Nitrate Vaginal Cream, 2% Formulations Condition: Vulvovaginal Candidiasis Date: 2009-12-23 Interventions:
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Completed |
Study Name: ProF-001_Phase IIa Condition: Vulvovaginal Candidiasis (VVC) Date: 2017-03-13 Interventions:
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Active, not recruiting |
Study Name: A Study to Evaluate Oral VT-1161 in the Treatment of Patients With Recurrent Vaginal Candidiasis (Yeast Infection) Condition: Recurrent Vulvovaginal Candidiasis Date: 2014-10-08 Interventions:
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Completed |
Study Name: Antimycotic Prophylaxis in Pediatric Patients Following Allogeneic Stem Cell Transplantation Condition:
Date: 2009-12-28 |
Completed |
Study Name: Safety of Pregnant Subjects Exposed to Ibrexafungerp Including Infant Outcomes Condition: Date: 2025-08-10 Interventions: This is not an interventional study |
Completed |
Study Name: Zinc-containing Vaginal Gel and Oral Fluconazole for Vulvovaginal Candidiasis. Condition: Date: 2025-08-10 Interventions: Women receive a single oral dose of fluconazole (150mg) followed by treatment with JUVIA zinc containing vaginal gel (daily for 2 weeks and twice per |
Completed |
Study Name: Evaluate the Efficacy and Safety of Ruxolitinib on Hair Regrowth in Patients With Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy (APECED)-Associated Alopecia Areata Condition: Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy (Apeced) Date: 2025-08-10 Interventions: Ruxolitinib (Jakafi) is approved by the FDA for the treatment of intermediate or high-risk myelofibrosis in adults, polycythemia vera in adults who ha |
NOT_YET_RECRUITING |
Study Name: Nitric Oxide Releasing Mouthwash (NORM) for the Management of Oropharyngeal Candidiasis Condition: Candidiasis, Oral Date: 2025-08-10 Interventions: Nitric Oxide Releasing Mouthwash will be self-administered by the participant three times throughout the day for 21 days.The intervention soluti |