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| Sponsor: | Oswaldo Cruz Foundation |
|---|---|
| Collaborator: |
Conselho Nacional de Desenvolvimento Científico e Tecnológico |
| Information provided by: | Oswaldo Cruz Foundation |
| ClinicalTrials.gov Identifier: | NCT00682656 |
Purpose
The adequate treatment of the American tegumentary leishmaniasis is crucial since the disease, differently from the caused by the Old World species, is painful and not self-healing and may lead to the disfiguring mucosal involvement. So far, pentavalents antimony compounds have been considered the treatment of choice for cutaneous leishmaniasis (CL), however, these drugs present high frequency of side effects and important disadvantages as parenteral administration and need for careful renal and cardiac monitoring. Azithromycin is a macrolide antibiotic, non-expensive, largely commercially available that has shown in-vitro and in vivo activity against different species of Leishmania.
The main objective of this study is to evaluate the efficacy and safety of oral azithromycin for the treatment of CL. The efficacy of oral treatment of azithromycin 500 mg/day for 20 days is going to be compared with the standard treatment of intramuscular injections of 20 mg/Kg/day of pentavalent antimonials (Glucantime®) for 20 days in patients with CL from two endemic regions of Brazil: the metropolitan region of Belo Horizonte in the southeast Brazil and in Corte de Pedras (Bahia), Northeastern Brazil. The patients follow up lasts for 12 months.
| Condition | Intervention | Phase |
|---|---|---|
|
Cutaneous Leishmaniasis |
Drug: N-metil glucamine Drug: Azithromycin |
Phase II Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study |
| Official Title: | Open Label Randomized Study to Assess Safety and Efficacy of Azithromycin Versus Meglumine Antimoniate to Treat Cutaneous Leishmaniasis |
| Estimated Enrollment: | 620 |
| Study Start Date: | June 2008 |
| Estimated Study Completion Date: | June 2010 |
| Estimated Primary Completion Date: | June 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
A: Active Comparator
N-metil glucamine
|
Drug: N-metil glucamine
N-metil glucamine (Glucantime®-Aventis) 15mg Sb+5/Kg/day, during 20 days. Maximum dose: 15ml/day
|
|
B: Experimental
Azithromycin
|
Drug: Azithromycin
Azithromycin (Zitromax®/ Pfizer) 500 mg per os 1x day, during 20 days
|
Eligibility| Ages Eligible for Study: | 14 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: Ana Rabello, MD, PhD | 55-31-3349-7708 | ana@cpqrr.fiocruz.br |
| Contact: Thais Amaral | 55-31-3349-7712 | amaralthais@cpqrr.fiocruz.br |
| Brazil, Minas Gerais | |
| Centro de Pesquisas René Rachou - Fiocruz | Recruiting |
| Belo Horizonte, Minas Gerais, Brazil, 30190-002 | |
| Contact: Álvaro Romanha romanha@cpqrr.fiocruz.br | |
| Principal Investigator: Ana Rabello, MD, PhD | |
| Sub-Investigator: Marcela Orsini, MD, PhD | |
| Sub-Investigator: Antonio Toledo, MD, MSc | |
| Sub-Investigator: Mariana Pedras, BSc, MSc | |
| Principal Investigator: | Ana Rabello, MD PhD | Oswaldo Cruz Foundation |
| Study Director: | Isabela Ribeiro, MD | Drugs for Neglected Diseases |
More Information
| Responsible Party: | Fundação Oswaldo Cruz ( Ana Rabello ) |
| Study ID Numbers: | CEPSH/CPqRR 21/2006 |
| Study First Received: | May 20, 2008 |
| Last Updated: | June 16, 2009 |
| ClinicalTrials.gov Identifier: | NCT00682656 History of Changes |
| Health Authority: | Brazil: National Health Surveillance Agency |
|
cutaneous leishmaniasis azithromycin N-metil glucamine |
|
Leishmaniasis Protozoan Infections Anti-Infective Agents Skin Diseases, Parasitic Skin Diseases Mastigophora Infections Leishmaniasis, Cutaneous |
Pharmacologic Actions Anti-Bacterial Agents Skin Diseases, Infectious Azithromycin Therapeutic Uses Sarcomastigophora Infections Parasitic Diseases |