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Safety of the Co-administration of Three Drugs for Trachoma and Lymphatic Filariasis Elimination (AZIVAL)

Primary Purpose

Parasitic Diseases, Bacterial Diseases

Status
Completed
Phase
Not Applicable
Locations
Mali
Study Type
Interventional
Intervention
triple co administration at once of the combination of Albendazole + ivermectin + azithromycin
Sponsored by
Centre d'Appui à la lutte contre la Maladie
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parasitic Diseases focused on measuring Albendazole, Ivermectin, Azithromycin, Lymphatic filariasis, Trachoma, Safety

Eligibility Criteria

5 Years - 65 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Must have been residing in the village for at least three months;
  • Must be 90 cm tall or more;
  • Must be between 5 years and 65 years of age;
  • Must not be pregnant;
  • Must not be lactating.

Exclusion Criteria:

  • Subjects under 5 years of age or less than 90 cm in height;
  • Subjects over 65 years of age;
  • Subjects who cannot swallow tablets;
  • Subjects who are sick and bedridden;
  • Pregnant women (clinical appreciation in the study);
  • Lactating women;
  • History of allergies to the drugs being studied (azithromycin, ivermectin, albendazole).

Sites / Locations

  • Centre National D'Appui a la lutte contre la Maladie

Outcomes

Primary Outcome Measures

Establish the incidence of adverse events associated with the mass triple drug administration

Secondary Outcome Measures

Establish the incidence of serious adverse events associated with the mass triple drug administration

Full Information

First Posted
April 23, 2012
Last Updated
April 24, 2012
Sponsor
Centre d'Appui à la lutte contre la Maladie
Collaborators
International Trachoma Initiative
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1. Study Identification

Unique Protocol Identification Number
NCT01586169
Brief Title
Safety of the Co-administration of Three Drugs for Trachoma and Lymphatic Filariasis Elimination
Acronym
AZIVAL
Official Title
A Pharmacovigilance Study on the Safety of Integrated Treatment of Trachoma and Lymphatic Filariasis in Children and Adults Living in the Sikasso Region of Mali
Study Type
Interventional

2. Study Status

Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
February 2010 (Actual)
Study Completion Date
February 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre d'Appui à la lutte contre la Maladie
Collaborators
International Trachoma Initiative

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether the triple co administration of albendazole, ivermectin and azithromycine is as safe as the current treatment scheme that consists to treat with albendazole plus ivermectin together and a week later to treat with azithromycin in areas co endemic for lymphatic filariasis and trachoma.
Detailed Description
Infectious diseases such as trachoma and lymphatic filariasis are public health problems in regions of Africa and Asia. Elimination programs exist for the two diseases, and their treatment by different groups of health workers is both costly and inefficient. Thus, a study evaluating the safety and feasibility of an integrated mass treatment of trachoma and lymphatic filariasis with azithromycin associated with albendazole and ivermectin was instituted in 4 villages of the region of Sikasso in Mali (West Africa) co endemic for lymphatic filariasis and trachoma. It was an open label randomized clusters type on the assessment of the safety of the triple co administration of azithromycin, ivermectin and albendazole (experimental regimen) as compared to the administration of the co administration of albendazole plus ivermectin followed by the that of azithromycin a week later (current standard recommended regimen) within subjects of 5 to 65 years old, willing and able to swallow the study drugs. Clinical evaluation of adverse events in all study participants was done on day 0, day 8, and day 15 after the treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parasitic Diseases, Bacterial Diseases
Keywords
Albendazole, Ivermectin, Azithromycin, Lymphatic filariasis, Trachoma, Safety

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
3000 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
triple co administration at once of the combination of Albendazole + ivermectin + azithromycin
Other Intervention Name(s)
Albendazole, Mectizan, Zithromax
Intervention Description
Albendazole 400mg + ivermectin according to the height + azithromycin according to the height at once
Primary Outcome Measure Information:
Title
Establish the incidence of adverse events associated with the mass triple drug administration
Time Frame
From Day 0 to Day 15 post treatment
Secondary Outcome Measure Information:
Title
Establish the incidence of serious adverse events associated with the mass triple drug administration
Time Frame
From Day 0 to Day 15 post treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Must have been residing in the village for at least three months; Must be 90 cm tall or more; Must be between 5 years and 65 years of age; Must not be pregnant; Must not be lactating. Exclusion Criteria: Subjects under 5 years of age or less than 90 cm in height; Subjects over 65 years of age; Subjects who cannot swallow tablets; Subjects who are sick and bedridden; Pregnant women (clinical appreciation in the study); Lactating women; History of allergies to the drugs being studied (azithromycin, ivermectin, albendazole).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Samba O Sow, MD, MPH
Organizational Affiliation
CNAM, Mali
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre National D'Appui a la lutte contre la Maladie
City
Bamako
Country
Mali

12. IPD Sharing Statement

Citations:
PubMed Identifier
23675549
Citation
Coulibaly YI, Dicko I, Keita M, Keita MM, Doumbia M, Daou A, Haidara FC, Sankare MH, Horton J, Whately-Smith C, Sow SO. A cluster randomized study of the safety of integrated treatment of trachoma and lymphatic filariasis in children and adults in Sikasso, Mali. PLoS Negl Trop Dis. 2013 May 9;7(5):e2221. doi: 10.1371/journal.pntd.0002221. Print 2013.
Results Reference
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Safety of the Co-administration of Three Drugs for Trachoma and Lymphatic Filariasis Elimination

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