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Effectiveness of traditional medicine products Juniperus excelsa M.Bieb in the treatment of cutaneous leishmaniasis

Determination of the efficacy of cryotherapy plus topical Juniperus excelsa M.Bieb, based on traditional Persian medicine, versus cryotherapy alone in the treatment of cutaneous leishmaniasis: a double-blind randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015082523753N1
Enrollment
60
Registered
2015-09-05
Start date
2015-10-07
Completion date
Unknown
Last updated
2018-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cutaneous leishmaniasis. Cutaneous leishmaniasis

Interventions

Intervention 1: Intervention group: cryotherapy as a standard treatment in addition to cream (topical pharmaceutical products) containing 5% extract of Juniperus excelsa M.Bieb adminnistrate, three t

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Age 18 to 70 years the maximum The maximum duration of their involvement by leishmaniasis is 4 months Having physical health except the cutaneous leishmaniasis infection Having 4 or less of the lesion leishmaniasis lesions Did not taking any of topical and systemic anti-Leishmania treatment during last 4 weeks Cutaneous leishmaniasis is approved of by smear

Exclusion criteria

Exclusion criteria: Patients with complex forms of leishmaniasis and symptoms of mucousal leishmaniasis Having more than 4 lesions The lesions greater than 5 cm Sub-cutaneous nodules Regional adenopaty if greater than 1 cm size Patients with immunodeficiency disease The infants and children less than 18 years Women in lactation and pregnancy Patients with satellite lesions or sporotrichoid lesions Patients with facial cutaneous leishmaniasis lesions

Design outcomes

Primary

MeasureTime frame
Size and area of leishmaniasis lesion. Timepoint: previous of the starting the treatment, weekly in the first month of treatment and every two weeks from second month to the end of the study. Method of measurement: Cooley and math with the square millimeters.

Secondary

MeasureTime frame
Duration of the healing the lesion. Timepoint: At the end of the treatment proccess. Method of measurement: The time interval between the beginning and end of treatment in days.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mohammad Mahdi Parvizi

Shiraz University of Medical Sciences

mmparvizi@gmail.com+98 71 3234 7966

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 26, 2026