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NCT03005353

Treatment of Candidal Vulvovaginitis Using Cumin Seed Extract Vaginal Suppositories.

Completed Phase 2, PHASE3 Last updated 9 June 2020
What this trial tests

Phase 2, PHASE3 trial testing Cumin seed extract in Infection, Fungal in 100 participants. Completed in 31 January 2020.

Timeline
1 March 2018
Primary endpoint
31 October 2019
31 January 2020

Quick facts

Lead sponsorAssiut University
PhasePhase 2, PHASE3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment100
Start date1 March 2018
Primary completion31 October 2019
Estimated completion31 January 2020
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

Adults 18 to 49, female only, with Infection, Fungal. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Fungal infections have increased over the last two decades, largely because of the increasing size of the population at risk, including patients who are immunocompromised, broad-spectrum antibiotics and intravascular catheter users. Essential oils and other extracts of plants have evoked interest as sources of natural products. They have been shown to possess antibacterial, antifungal, antiviral, insecticidal and antioxidant properties. To the best of our knowledge, no study has examined the efficacy of cumin seed extract on relieving vulvovaginal candidiasis in vivo.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Infection, Fungal

Currently open trials in the same condition.

Other Assiut University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03005353.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing