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Evaluation of the effectiveness of oral dapsone with intralesional antimoniate in treatment of cutaneous leishmaniasis

Evaluation of the effectiveness of oral dapsone with intralesional antimoniate in treatment of cutaneous leishmaniasis in comparison with intralesional antimoniate alone

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140211016554N4
Enrollment
100
Registered
2019-04-28
Start date
2013-01-20
Completion date
Unknown
Last updated
2019-05-21

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: In control group, patients receive intralesional glucantime injection weekly for 4-8 weeks. Intervention 2: In intervention group, weekly intralesional injection of glucantime starts f

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 40 Years

Inclusion criteria

Inclusion criteria: positive direct smear of the lesion in terms of leishman bodies patient has indication of topical treatment according to the physician less than six month has elapsed since the manifestation of lesion patient has not received any previous treatment for cutaneous leishmaniasis intervention group has normal values for CBC;G6PD;LFT location of lesion is either on upper limbs or face

Exclusion criteria

Exclusion criteria: sensitivity to glucantime (severe topical reaction, anaphylaxis). absence of regular follow-ups existence of secondary infection in lesion use of other treatments during the study dapsone side effects including methemoglobinemia, hemolytic anemia, agranulocytosis, peripheral neuropathy, hypersensitivity

Design outcomes

Primary

MeasureTime frame
Change in size of the lesion. Timepoint: At the end of each week. Method of measurement: based on lesion induration measured by a caliper.

Secondary

MeasureTime frame
Side effects. Timepoint: weekly. Method of measurement: clinical evaluation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzadeh Mohammadi

Mashhad University of Medical Sciences

src@mums.ac.ir+98 51384012493

Outcome results

None listed

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