Mefloquine Prophylaxis in HIV-1 Individuals: a Randomized Placebo-controlled Trial
Study Details
Study Description
Brief Summary
This is a randomized placebo controlled trial. Malaria chemoprophylaxis with mefloquine in asymptomatic HIV-infected adults living in a malaria endemic region of Luanshya, Zambia will be compared to a placebo control group and followed up for 18 months.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
In Zambia prompt treatment of malaria cases is the mainstay of malaria control; antimalarial chemoprophylaxis is not currently recommended for general use so that the use of placebo as a comparator in this study is justified. We will analyse safety and efficacy of mefloquine, malaria and AIDS related parameters at predefined time points, and verify if this intervention could produce a slower decrease in CD4 counts compared to passive case management of malaria.
This is a randomized placebo controlled trial. Malaria chemoprophylaxis with mefloquine in asymptomatic HIV-infected adults living in a malaria endemic region of Luanshya, Zambia will be compared to a placebo control group and followed up for 18 months.
Specific designed studies taking into account possible confounding parameters (and interactions) are needed to measure the impact of malaria control in an HIV endemic environment. In particular, the question should be answered if malaria control has an impact on the disease progression of HIV. The possible impact of these interventions on morbidity and mortality taking into account these parameters might have a major public health impact. This might be on the use of antiretroviral drugs, the incidence of clinical (eventually severe) malaria and spread of antimalarial resistance through immune compromised HIV patients (with and without antimalarial treatment).
Studies of alternative strategies that contribute (next to antiretrovirals) to the control and prevention of HIV pandemic are equally important and urgently needed. The need to design these strategies is critical given the high incidence of malaria and HIV in countries in Sub Saharan Africa such as Zambia and its serious impact on survival and the socio-economic situation. Moreover, a cost-benefit analysis might show that some alternative strategies have a major impact on the field with less technical, financial and social constraints than the strategies recommended so far.
All HIVP patients will be treated for opportunistic infections (OI) and receive antiretroviral drugs following the National guidelines on Management and Care of Patients with HIV/AIDS (also if this occurs after the study period). At the time they need cotrimoxazole prevention or/and receive antiretrovirals they would have reached a study endpoint and will be excluded from the trial though the follow up will continue.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Placebo Comparator: Placebo, tablet
|
Drug: placebo
tablet, once weekly
|
| Experimental: mefloquine, tablet
|
Drug: mefloquine
tablet, once weekly
|
Outcome Measures
Primary Outcome Measures
- Rate of decline of CD4 counts between different time points [months 0, 6, 12 and 18]
- Proportion of patients entering the AIDS stage (WHO stage 3,4) [during 18 months]
Secondary Outcome Measures
- Mean difference in log plasma viral load at different time points, [during 18 months]
- Rate of decline of humoral immunity between different time points. [during 18 months]
- Proportion of patients with parasitaemia at the end of the intervention. [during 18 months]
- All cause disease incidence and prevalence (including malaria, TB) [during 18 months]
- Proportion of patients with Adverse event during monitoring [during 18 months]
- Prevalence of anaemia at different time points [during 18 months]
- Incidence of severe anaemia [during 18 months]
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Permanent residents of the Luanshya district
-
Males and non pregnant adults between 18 and 50 years old.
-
Having a CD4 cell count of least 350 perµL at enrolment
-
HIV sero-status determined at the VCT of the health center.
-
No obvious underlying disease at time of enrolment
-
Signed informed consent
Exclusion Criteria:
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HIV stage III or IV following the WHO classification (see attached documents regarding policy in Zambia)
-
Evidence of underlying chronic diseases (cardiac, renal, hepatic, malnutrition, TB).
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Intent to move out of the study catchment area during the study period
-
History of allergy to MQ (or related drugs) or sulfa drugs
-
Chorionic gonadotrophic hormone in urine or obvious pregnancy
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Tropical Disease Research Center | Ndola | Cupperbelt | Zambia |
Sponsors and Collaborators
- Institute of Tropical Medicine, Belgium
Investigators
- Study Director: Umberto D'Alessandro, MD,MSc, PHD, Institute of Tropical Medicine Antwerp
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- Mefloquine HIV zambia