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Mefloquine Prophylaxis in HIV-1 Individuals: a Randomized Placebo-controlled Trial

Information source: Institute of Tropical Medicine, Belgium
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: HIV Infections

Intervention: mefloquine (Drug); placebo (Drug)

Phase: N/A

Status: Completed

Sponsored by: Institute of Tropical Medicine, Belgium

Official(s) and/or principal investigator(s):
Umberto D'Alessandro, MD,MSc, PHD, Study Director, Affiliation: Institute of Tropical Medicine, Antwerp

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.

Clinical Details

Official title: Mefloquine Malaria Prophylaxis in HIV-1 Infected Individuals and Its Influence on the Evolution Towards AIDS: a Randomized Placebo-controlled Trial

Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Primary outcome:

Rate of decline of CD4 counts between different time points

Proportion of patients entering the AIDS stage (WHO stage 3,4)

Secondary outcome:

Mean difference in log plasma viral load at different time points,

Rate of decline of humoral immunity between different time points.

Proportion of patients with parasitaemia at the end of the intervention.

All cause disease incidence and prevalence (including malaria, TB)

Proportion of patients with Adverse event during monitoring

Prevalence of anaemia at different time points

Incidence of severe anaemia

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.

Eligibility

Minimum age: 18 Years. Maximum age: 50 Years. Gender(s): Both.

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 per┬ÁL 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:

- 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).

- 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

Locations and Contacts

Tropical Disease Research Center, Ndola, Cupperbelt, Zambia
Additional Information

Starting date: October 2005
Last updated: May 23, 2011

Page last updated: August 23, 2015

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