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Arnica Tincture Fot the Treatment of Cutaneous Leishmaniasis

Study acronym: ARNICA
StatusActive, Not Recruiting
PhasePhase 1
Started
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Record History

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  1. Notable Primary completion date changed from estimate of Nov 2023 to Nov 2, 2024
    • Trial status: Recruiting to Active, Not Recruiting
    • Study completion date: May 2024 to Aug 2025
    • Site details revised
    v4
  2. Notable Phase: Phase 1/2 to Phase 1v3 Show 5 more changesShow less
    • Trial status: Not Yet Recruiting to Recruiting
    • Primary completion date: Apr 2023 to Nov 2023
    • Start date changed from estimate of Jan 2023 to May 3, 2023
    • Study completion date: Apr 2024 to May 2024
    • Site details revised
  3. Notable Primary completion date: Apr 2022 to Apr 2023v2 Show 5 more changesShow less
    • Start date: Jan 2022 to Jan 2023
    • Primary endpoint revised
    • Study completion date: Apr 2023 to Apr 2024
    • Secondary endpoints revised (2)
    • Study description shortened, about 355 words
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Cutaneous Leishmaniasis (CL) is a parasitic disease caused by more than 20 different species of the protozoan parasite Leishmania. CL generally begins with a papule at the sand fly bite site, increasing to form a nodule that progresses to ulceration, or a scaly or wart-like plaque, over a period of 1 to 3 months. The exact incidence of CL is not known. An estimated 1.2 million cases / year in approximately 100 countries around the world suffer from different forms of CL. In general, most lesions become ulcerated during the course of the disease. Among the different species of the parasite that cause LC, L. tropica from the Old World and L. braziliensis from the New World are considered the most important due to the severity of the disease they produce and because they are more difficult to cure with medications currently available. Since 2010, the World Health Organization has insisted on the need to work on products that become alternatives for the treatment of CL, especially in products that serve topical application because with them, the probability of systemic toxicity is lower , increasing patient safety. Among the options for topical treatment are natural products that have been, are, and will be extremely important as sources of medicinal agents. In addition to natural products that have found direct medicinal application as pharmaceutical entities, many others can serve as chemical models or templates for the design, synthesis and semi-synthesis of novel substances for the treatment of human diseases. Arnica montana L. is a plant with anti-echemotic, healing, anti-inflammatory, analgesic and antineuralgic properties; It is included in the Colombian vademecum of medicinal plants. In previous studies it has been observed that the contact of the ulcerated skin with the product for up to 60 days does not generate toxic effects at the local level (application site) or at the systemic level, so it can be considered safe for use. To date there are no human studies with CL. Therefore, it is intended to evaluate the safety and tolerability of Arnica tincture in individuals with uncomplicated CL, by measuring the occurrence and severity analysis of local and systemic adverse events.
Trial Details
NCT Number NCT05094908
Lead Sponsor Universidad de Antioquia
Collaborators: INNOVATION CORPORATION FOR THE DEVELOPMENT OF PRODUCTS FOR TROPICAL DISEASES (CIDEPRO)
Conditions
(from sponsor)
Leishmaniasis, Cutaneous
Related terms Leishmaniasis, Leishmaniasis, Cutaneous
Enrollment 16 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov