HIV/AIDS
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Being HIV sero-positive 2. Patients = 18 years old 3. Patients with CD4 counts = 500 cells/mm3 4. Commenced ART at least for three months (Tenofovir + Lamivudine + Efavirenz combination). 5. Be willing to give informed consent and comply with study protocol
Exclusion criteria
Exclusion criteria: 1. Known allergy or intolerance to Moringa oleifera or placebo (cornstarch powder) 2. Pregnant women 3. Patients with CD4 counts > 500 cells/mm3 4. Patients with active opportunistic infection 5. Patients taking anti-coagulant, micronutrient or natural health product supplements within 30days of randomization 6. Patients with poor or suboptimal adherence to ART medication 7. For ease of monitoring and to achieve maximum compliance to study protocol, patients living outside Kano metropolis will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in immunological status: a.CD4;Change in immunological status: b. Viral load ;Change in anthropometric parameters ( weight, BMI, waist-hip circumference & mid-arm circumference); Occurrence and frequency of opportunistic infections | — |
Secondary
| Measure | Time frame |
|---|---|
| Patients’ quality of life (QoL) | — |
Countries
Nigeria
Contacts
Supervisor