Leishmaniasis, Cutaneous
Conditions
Keywords
cutaneous leishmaniasis of the old world
Brief summary
Background: Cutaneous Leishmaniasis is a worldwide disease, endemic in over 88 countries, that has shown an increasing incidence over the last many decades. For the last 60 years antimony compounds are considered the treatment of choice. Though their use is expensive, cumbersome, has many adverse effects and not effective in all patients, the search for a better alternative is still going on. Low dose antimony compounds in combination with several agents have shown promise of reducing adverse effects of antimony compounds without compromising efficacy. Allopurinol is one such agent which though promising lacks randomized, controlled trials to prove efficacy. The main objective of this study is to evaluate low dose sodium stibogluconate in combination with allopurinol and to compare it with high dose sodium stibogluconate in terms of efficacy and adverse effects. Methods and design: A multi-center randomized, controlled trial including 620 patients from endemic areas for Leishmaniasis in Pakistan will be undertaken to assess the research question. Parasitologically confirmed cutaneous leishmaniasis will be included in the study. After evaluating the inclusion/exclusion criteria patients will be randomized to receive either meglumine antimoniate (20 mg/kg/day/intramuscular, till clinical resolution or a maximum of 28 days) or combination of meglumine antimoniate (10 mg/kg/day intramuscular) and allopurinol (20 mg/kg/day/oral) till clinical resolution or a maximum of 28 days. During treatment patients will be admitted to hospital and monitored daily for the presence of adverse effects. Follow up period will last six months during which patients will visits the research centers for assessment of healing process at monthly intervals.
Interventions
DRUGmeglumine antimoniate, allopurinol
first drug in injectable, second is in tablet form.
injectable 20 mg/kg/day/intramuscular for 21 days.
Sponsors
Combined Military Hospital, Pakistan
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No
Inclusion criteria
* Men and women between 18 and 50 years old. * Cutaneous ulcers, nodules, plaques, of more than two weeks of evolution requiring systemic therapy. * Positive parasitological diagnosis for cutaneous leishmaniasis. * Patients that voluntarily accept to participate in the study and sign the informed consent. * Disposition to be admitted to hospital, if necessary, and to attend all the visits punctually (initial, treatment and follow up). * Acceptation of not using any other treatment for cutaneous leishmaniasis while in the study.
Exclusion criteria
* Pregnant women. * Presence of any condition or disease that compromises the patient immunologically (i.e. diabetes, cancer, etc.) or, any other, that, based on the judgment of the researcher, could alter the course of cutaneous leishmaniasis. * Diffuse cutaneous leishmaniasis. * Visceral leishmaniasis. * Complete or incomplete treatment with antimony compounds in the last three months. * Patients with history of hepatic, renal, or cardiovascular disease. * Mentally or neurologically disabled patients that are considered not fit to approve their participation in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| clinical healing of lesions. | 3 months |
Secondary
| Measure | Time frame |
|---|---|
| improvement of more than 50% in lesion size | 3 months |
Countries
Pakistan
Outcome results
None listed