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Topical treatment of cutaneous leishmaniasis with lipozomal azithromycin

Evaluation of topical liposomal azithromycin for treatment of acute cutaneous leishmaniasis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014031216955N1
Enrollment
66
Registered
2014-05-16
Start date
2009-10-01
Completion date
Unknown
Last updated
2018-02-22

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: use of topical liposomal Azithromycin twice daily for 6 weeks. Intervention 2: Control group: injection of intralesional meglumine antimoniate (glucantime) weekly f
Treatment - Drugs
Intervention group: use of topical liposomal Azithromycin twice daily for 6 weeks
Control group: injection of intralesional meglumine antimoniate (glucantime) weekly for 6 weeks

Sponsors

Mashhad University of Medical Sciences, Vice Chancellor for Research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Presence of cutaneous leishmaniasis with less than 12 weeks of clinical course; Not receive any treatment before Exclusion criteria: Pregnancy; Lactating; Receiving simultanous treatment with other methods during treatment course; Sensitivity or intolerance to Macrolids; History of significance renal; Pulmonary and cardiovascular disease

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Lesion improvement. Timepoint: Weekly until 6 weeks. Method of measurement: Measuring the size of induration and ulcer by caliper.

Secondary

MeasureTime frame
Side effects. Timepoint: Weekly. Method of measurement: Clinical evaluation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Pouran layegh

Cutaneous Leishmaniasis Research center, Mashhad University of Medical Sciences

layeghpo@mums.ac.ir+98 51 1801 2851

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026