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Liposomal Amphotericin in Disseminated Leishmaniasis

Primary Purpose

Disseminated Leishmaniasis

Status
Completed
Phase
Phase 3
Locations
Brazil
Study Type
Interventional
Intervention
Liposomal Amphotericin B
Sponsored by
Hospital Universitário Professor Edgard Santos
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Disseminated Leishmaniasis focused on measuring Disseminated leishmaniasis, Liposomal Amphotericin B, Leishmania braziliensis

Eligibility Criteria

14 Years - 80 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • a) clinical diagnosis of Disseminated Leishmaniasis according to case definition; b) illness duration of less than three months, c) parasite identification by culture or polymerase chain reaction methods, d) no previous treatment for leishmaniasis.

Exclusion Criteria:

  • a) immunodeficiency or antibodies to HIV, b) pregnancy or patients not willing or unable to use contraceptives during and 3 months after the end of therapy c) ALT, AST ≥3x normal reference values, creatinine and BUN ≥1.5x normal reference values, d) any evidence of serious underlying disease (cardiac, renal, hepatic, or pulmonary) including serious infection other than DL.

Sites / Locations

  • HUPES

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Liposomal Amphotericin

Arm Description

Liposomal Amphotericin by intravenous route, 3 to 5 mg/kg/day, during 7 to 14 days of treatment.

Outcomes

Primary Outcome Measures

Definitive cure
Definitive cure at 3 months after the end of treatment is defined as complete epithelialization of all ulcers and complete disappearance of inflammatory infiltrations from all lesions.

Secondary Outcome Measures

Toxicity
Evaluation of side effects and laboratory parameters during the 7 to 15 days of treatment.

Full Information

First Posted
December 26, 2013
Last Updated
December 30, 2013
Sponsor
Hospital Universitário Professor Edgard Santos
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1. Study Identification

Unique Protocol Identification Number
NCT02025491
Brief Title
Liposomal Amphotericin in Disseminated Leishmaniasis
Official Title
Efficacy Study of Liposomal Amphotericin in Disseminated Leishmaniasis
Study Type
Interventional

2. Study Status

Record Verification Date
December 2013
Overall Recruitment Status
Completed
Study Start Date
April 2011 (undefined)
Primary Completion Date
February 2013 (Actual)
Study Completion Date
August 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitário Professor Edgard Santos

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Disseminated leishmaniasis (DL) is an emerging and severe form of leishmaniasis, with increasing prevalence in Bahia, Brasil. It is characterized by multiple acneiform, papular and ulcerated lesions localized on the face, chest, abdomen and extremities. The number of lesions ranges from 10 to hundreds, and mucosal disease has been documented in more than 40% of the cases. DL is a hard to cure disease and therapeutic failure with pentavalent antimony has been documented in up to 70% of the cases caused by L. braziliensis in the endemic area of Corte de Pedra, Bahia. The majority of DL patients need several courses of antimony or the use of high dose of Amphotericin B desoxicolate to cure. Therefore DL patients are exposed to relevant drug toxicity, high morbidity due to a long lasting disease, with an important socio-economic impact. Our hypothesis is that liposomal Amphotericin B has a higher cure rate than historic cure rates of pentavalent antimony in the treatment of disseminated leishmaniasis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Disseminated Leishmaniasis
Keywords
Disseminated leishmaniasis, Liposomal Amphotericin B, Leishmania braziliensis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Liposomal Amphotericin
Arm Type
Experimental
Arm Description
Liposomal Amphotericin by intravenous route, 3 to 5 mg/kg/day, during 7 to 14 days of treatment.
Intervention Type
Drug
Intervention Name(s)
Liposomal Amphotericin B
Other Intervention Name(s)
Ambisome
Intervention Description
Liposomal Amphotericin B will be administered by intravenous route, 3 to 5 mg/kg/day, during 7 to 14 days of treatment. Complete hemogram, aminotransferases (AST, ALT), blood urea and creatinine will be determined in all patients on days -1, and three times/week up to the end of therapy. Patients will bemonitored for side effects daily. Patients will be followed-up at 1, 2, 3, 4 and 6 months post-therapy. Clinical and laboratory adverse events will be graded according to the Common Toxicity Criteria (CTC) of the National Cancer Institute.
Primary Outcome Measure Information:
Title
Definitive cure
Description
Definitive cure at 3 months after the end of treatment is defined as complete epithelialization of all ulcers and complete disappearance of inflammatory infiltrations from all lesions.
Time Frame
3 months after treatment
Secondary Outcome Measure Information:
Title
Toxicity
Description
Evaluation of side effects and laboratory parameters during the 7 to 15 days of treatment.
Time Frame
During the 7 to 15 days of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: a) clinical diagnosis of Disseminated Leishmaniasis according to case definition; b) illness duration of less than three months, c) parasite identification by culture or polymerase chain reaction methods, d) no previous treatment for leishmaniasis. Exclusion Criteria: a) immunodeficiency or antibodies to HIV, b) pregnancy or patients not willing or unable to use contraceptives during and 3 months after the end of therapy c) ALT, AST ≥3x normal reference values, creatinine and BUN ≥1.5x normal reference values, d) any evidence of serious underlying disease (cardiac, renal, hepatic, or pulmonary) including serious infection other than DL.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paulo RL Machado, MD PhD
Organizational Affiliation
UFBA
Official's Role
Principal Investigator
Facility Information:
Facility Name
HUPES
City
Salvador
State/Province
Bahia
ZIP/Postal Code
40000
Country
Brazil

12. IPD Sharing Statement

Citations:
PubMed Identifier
26048961
Citation
Machado PR, Rosa ME, Guimaraes LH, Prates FV, Queiroz A, Schriefer A, Carvalho EM. Treatment of Disseminated Leishmaniasis With Liposomal Amphotericin B. Clin Infect Dis. 2015 Sep 15;61(6):945-9. doi: 10.1093/cid/civ416. Epub 2015 Jun 5.
Results Reference
derived

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Liposomal Amphotericin in Disseminated Leishmaniasis

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