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Safety and Efficacy of Azithromycin to Treat Cutaneous Leishmaniasis (PCL01)
This study is currently recruiting participants.
Verified by Oswaldo Cruz Foundation, June 2009
First Received: May 20, 2008   Last Updated: June 16, 2009   History of Changes
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

Resource links provided by NLM:


Further study details as provided by Oswaldo Cruz Foundation:

Primary Outcome Measures:
  • Proportion of clinically cured patients [ Time Frame: at the third month after treatment ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Proportion of patients with failure [ Time Frame: twelve months after treatment ] [ Designated as safety issue: No ]
  • Occurrence of mucosal lesions after treatment [ Time Frame: twelve months after treatment ] [ Designated as safety issue: No ]
  • Proportion of patients presenting new lesions [ Time Frame: 1st 2nd 3rd 6th 12th month after treatment ] [ Designated as safety issue: No ]
  • Proportion of adverse events on each treatment group [ Time Frame: 1st 2nd 3rd 6th 12th month after treatment. ] [ Designated as safety issue: Yes ]

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
Criteria

Inclusion Criteria:

  • Patients older than 14 and younger than 65 years old
  • Skin lesions with clinical suggestion of cutaneous leishmaniasis and positive leishmanin skin test (Montenegro test)
  • Agreement to participate in the study and signed the informed consent

Exclusion Criteria:

  • Diabetes mellitus, kidney diseases, liver or cardiac diseases, tuberculosis, malaria.
  • Pregnancy
  • Breast feeding
  • Cutaneous lesion with bacterial infection for which antibiotics need to be prescribed
  • More than six cutaneous lesions
  • Previous history of cutaneous or mucosal leishmaniasis
  • Use of drugs with potential pharmacological interactions with antimonials as anti-arrhythmic or tricycle anti-depressives
  • Previous intolerance to azithromycin or other macrolides or N-metilglucamine
  • Abusive alcohol ingestion according to the CAGE questionnaire
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00682656

Contacts
Contact: Ana Rabello, MD, PhD 55-31-3349-7708 ana@cpqrr.fiocruz.br
Contact: Thais Amaral 55-31-3349-7712 amaralthais@cpqrr.fiocruz.br

Locations
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            
Sponsors and Collaborators
Oswaldo Cruz Foundation
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Investigators
Principal Investigator: Ana Rabello, MD PhD Oswaldo Cruz Foundation
Study Director: Isabela Ribeiro, MD Drugs for Neglected Diseases
  More Information

No publications provided

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

Keywords provided by Oswaldo Cruz Foundation:
cutaneous leishmaniasis
azithromycin
N-metil glucamine

Additional relevant MeSH terms:
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

ClinicalTrials.gov processed this record on February 04, 2010