Intralesional Antimony for Bolivian Cutaneous Leishmaniasis

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-01-31

Study Completion Date

2012-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Intralesional injection of antimony has been used for L major from Iran with a modest cure rate \[56%: Asilian 2004\]. However, this therapeutic approach has been used for L braziliensis from Brazil, with an attractive cure rate after 3 months of 80% \[Oliveira-Neto 1997\]. Because intralesional Sb injections is the local therapy with the best reported cure rate for South American L braziliensis disease, the species that causes disease in Bolivia, this pilot study of local therapy for bolivian L braziliensis disease will evaluate intralesional Sb therapy.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Topical Paromomycin for Cutaneous Leishmaniasis in Bolivia

NCT03096457

Leishmaniasis, Cutaneous Leishmania Braziliensis Complex Leishmaniasis, American +1 more

COMPLETED PHASE2/PHASE3

Treatment of Cutaneous Leishmaniasis With a Combination of Miltefosine and Antimony

NCT01380301

Cutaneous Leishmaniasis

TERMINATED PHASE2

Oral Miltefosine Plus Topical Imiquimod to Treat Cutaneous Leishmaniasis

NCT01380314

Cutaneous Leishmaniasis

COMPLETED PHASE2

Short Course of Miltefosine and Antimony to Treat Cutaneous Leishmaniasis in Bolivia

NCT00537953

Cutaneous Leihmaniasis

UNKNOWN PHASE2

Miltefosine to Treat Cutaneous Leishmaniasis in Bolivia

NCT00233545

Cutaneous Leishmaniasis

COMPLETED PHASE2

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Cutaneous leishmaniasis is endemic in the New World from approximately the US-Mexican border through Central America and the Northern part of South America down to the level of Rio de Janeiro.

Until recently, the standard treatment for the leishmaniases was pentavalent antimony (Glucantime or Pentostam). The cure rate for L panamensis in Colombia is 91%-93% \[Soto, 1993; Velez, 1997\], a large study with several formulations of antimony found a combined Bolivia-Colombia cure rate of 86% \[Soto, 2004b\], and the cure rate in Palos Blancos, Bolivia is 15 of 16 = 94% \[ Soto, 2008\]. Nevertheless, pentavalent antimonials have the disadvantages of multiple injections during at least 3 weeks and mild-moderate clinical toxicity: local pain at the site of injections and generalized myalgias and arthralgias that can be severe and responsible for partial or definitive interruption of therapy, gastrointestinal complaints, liver enzyme elevations, pancreatic enzyme elevations and more rarely but with danger for life ventricular repolarization problems \[Soto, 2005, Velez 2010\], all of which are particularly unpleasant for a localized moderate clinical problem such as cutaneous leishmaniasis that usually is not dangerous for the patient.

The oral agent Miltefosine has now been shown to be as effective as antimony in Colombia and Bolivia. In Colombia, the cure rate for miltefosine was 91% \[Soto 2004a\] and in the just-completed trial in Palos Blancos, the cure rate for miltefosine was 32 of 37 = 88 % . Side effects seen in patients with cutaneous disease that can be specifically attributed to the drug are nausea and vomiting of mild grade in approximately 25% of patients, and low-grade elevation of creatinine also in approximately 25% of patients \[Soto 2001; Soto 2004\]. Now that cutaneous leishmaniasis is affecting more women at reproductive age, there is a crucial inconvenient because miltefosine can't be taken during pregnancy and breastfeeding; additionally prolonged courses (4 weeks) makes more difficult adherence to therapy and emerge the risk of incomplete treatments or it might be necessary supervised administration during the full course.

For small, single lesions, the side effects and cost of systemic therapy with antimony or miltefosine may outweigh the advantage of cure. For such lesions, targeted local therapy would be attractive if it is effective. The cost of goods will be low, and systemic adverse events would be non-existent.

For these reasons, topical treatment of the leishmaniases is presently the subject of intense worldwide interest, including at a recent \[July 2010\] PAHO meeting in Colombia. The leading candidates are topical formulations of paromomyin, local heat since cutaneous leishmania are heat-sensitive, local freezing as per any dermatologic lesion, and intralesional injections of antimony. The ability of topical formulations of paromomycin to cure depends on penetration of this divalent cation into the lesion and thus depends on the precise formula for the cream in which the paromomycin is dissolved. Other than the combination of paromomycin plus MBCL in Vaseline, which had minimal efficacy in Colombia \[Soto 1998\], patented paromomycin-containing creams are under investigation but cannot be obtained except from Pharma. Reports of local thermotherapy have been published, but again the key issue is penetration of the agent \[in this case, heat\] to the lesion and the best approach is difficult to utilize because it requires a $25,000 machine and exists a risk of infections via electrodes.

Intralesional injection of antimony has also been used for L major from Iran, and also with a modest cure rate \[56%: Asilian 2004\]. However, this therapeutic approach has been used for L braziliensis from Brazil, with an attractive cure rate after 3 months of 80% \[Oliveira-Neto 1997\]. Because intralesional Sb injections is the local therapy with the best reported cure rate for South American L braziliensis disease, the species that causes disease in Bolivia, this pilot study of local therapy for bolivian L braziliensis disease will evaluate intralesional Sb therapy.

Cryotherapy has been used as sole therapy for L major from Iran. The cure rate was modest: 50-60% \[Asilian 2004; Layegh 2009\]. Nevertheless, cryotherapy may have an attractive cure rate against L braziliensis. Therefore, cryotherapy will also be evaluated in this pilot study.

Patients receiving intralesional Sb will be randomized vs vs patients receiving cryotherapy and also vs patients receiving an emollient cream Because Il Sb has perhaps more promise than cryotherapy, more patients will receive Il Sb (30) than will receive cryotherapy (20) The emollient cream may improve host response to the trauma of the parasitic process, nevertheless, emollient cream is a placebo treatment in the specifically antiparasitic sense. The spontaneous rate of cure is unknown in Bolivia, thus this group will serve to establish this key value and permit comparison of the IL Sb rate and the cryotherapy rate to it. Although 20 patients will be randomized to the "placebo" group, stopping rules are such that if 4 early patients or 6 total patients in this group fail, no further "placebo" patients will be entered into the trial.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Leishmaniasis Cutaneous Leishmaniasis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Intralesional antimony

3 intralesional injections of antimony at D1, D3 and D7

Group Type EXPERIMENTAL

pentavalent antimony

Intervention Type DRUG

3 intralesional injections of antimony at D1, D3 and D7

Cryotherapy

Liquid nitrogen until freezing at DF1 and D14

Group Type ACTIVE_COMPARATOR

cryotherapy

Intervention Type PROCEDURE

Frozing of lesions with liquid nitrogen ad D1 and D14

Topical cream

topical treatment 3 times a day during 21 days with an emollient cream

Group Type PLACEBO_COMPARATOR

placebo cream

Intervention Type DRUG

topical emollient crean 3 times a day during 21 days

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

pentavalent antimony

3 intralesional injections of antimony at D1, D3 and D7

Intervention Type DRUG

cryotherapy

Frozing of lesions with liquid nitrogen ad D1 and D14

Intervention Type PROCEDURE

placebo cream

topical emollient crean 3 times a day during 21 days

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Gender: Male or female
* Age: \>12 yrs of age
* Clinicla presentation: 1-2 ulcerative lesions, each \< 30 mm in largest diameter, and with a total lesion area \<900 mm2.
* Parasitological confirmation of the lesion will be made by visualization or culture of leishmania from the biopsy or aspirate of the lesion.

Exclusion Criteria

* Previous treatment for leishmaniasis: therapy with Sb, pentamidine, amphotericin B, miltefosine, imidazoles or allopurinol in the last 3 months
* Concomitant diseases by history that would be likely in the PI's opinion to interact, either positively or negatively, with IL Sb treatment.

Minimum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No