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Efficacy of Higher Albendazole and Ivermectin Doses on Wuchereria Bancrofti Microfilarial Clearance in Malawi

Registration Number
NCT01213576
Lead Sponsor
London School of Hygiene and Tropical Medicine
Brief Summary

Albendazole and ivermectin are currently used in combination for annual mass treatment of lymphatic filariasis in Africa. Although the drugs have been donated, the cost of such programmes is very high and has proven to be a major impediment to the success of programmes in many countries with limited financial resources.

Data from albendazole treatment of other filarial infections and one study comparing single to multi-dose Diethycarbamazine/albendazole in lymphatic filariasis suggest that increased dose and/or frequency of albendazole dosing may be more effective in clearing microfilariae. It is essential to determine whether such higher doses are indeed beneficial since this could have far-reaching effects on the conduct and management of the main mass treatment programmes and also in the management of programmes as they near elimination.

Detailed Description

The proposed study will enrol up to 120 volunteers with microfilaremic Wuchereria bancrofti infection who would be randomized to receive standard annual treatment (albendazole 400 mg + ivermectin 200 mcg/kg), annual treatment with an increased dose of albendazole (albendazole 800 mg + ivermectin 200400 mcg/kg) or semi-annual treatment with a standard (albendazole 400 mg + ivermectin 200 mcg/kg), or an increased albendazole dose (albendazole 800 mg + ivermectin 200 400 mcg/kg). Microfilarial levels, as well as measures of adult worm burden (circulating antigen) will be followed every six months for two years to determine whether the higher doses, or more frequent regimens are more effective.

The data obtained would be used, in combination with the data from other similar studies being conducted in Mali and in India to advise the Global Programme for the Elimination of Lymphatic Filariasis (GPELF) on improved methods of treatment both for mass treatment and for the management of problem areas within the global programme.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
70
Inclusion Criteria
  • understand and sign informed consent
  • willing to undergo night blood sampling every 6 months for 2 years
  • Age 18 to 55 years
  • Haemoglobin of equal or above 9g/dl
  • Microfilarial level of equal or above 80mg/dl
Exclusion Criteria
  • Non- consenting
  • Pregnancy or lactation
  • Treatment with albendazole or ivermectin within the previous 6 months
  • Known allergy to the study drugs

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Albendazole 400mg and ivermectin 200mcg/kgAlbendazole 400mg and ivermectin 200mcg/kgalbendazole 400mg and ivermectin 200mcg/kg given twice a year
albendazole 400mg and ivermectin 200mcg/kgAlbendazole 400mg and ivermectin 200mcg/kgAnnual treatment
Albendazole 800mg and ivermectin 400mcg/kgAlbendazole and ivermectinAnnual treatment
Albendazole 800mg and ivermectin 400mcg /kg bi-annuallyalbendazole 800mg and ivermectin 400mcg/kg bi-annuallyAlbendazole 800mg and ivermectin 400mcg/kg given twice a year
Primary Outcome Measures
NameTimeMethod
Number of Participants Achieving Microfilarial Clearance12 months

Microfilaria clearance will be assessed in regard to dosage as well as frequency of treatment. Microfilarial clearance is defined by non-detection of microfilaria in the night blood sample.

Secondary Outcome Measures
NameTimeMethod
Number of Participants With Microfilarial Clearance at 24 Months of Follow up24 months

Microfilaria will be detected using the nucleopore filtration technique and analysed according to the respective treatment arms at the 24 month time point. Microfilarial clearance will be defined by non-detection of microfilaria in the night blood sample

Trial Locations

Locations (1)

Karonga Prevention Study

🇲🇼

Karonga, Malawi

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