HIV Infections Clinical Trial
Official title:
Can Anthelminthic Treatment Delay the Progression of HIV? Randomised Open-label Trial Testing Presumptive Anthelminthic Treatment on Progression of HIV in ART-naïve HIV-positive Patients in a Rural African Setting With Presumed High Prevalence of Helminth Infections.
This study focuses on one of the major health issues of Sub-Saharan Africa: multi-parasitism
and co-infections. In particular this study aims to elucidate the interaction of helminths
with HIV.
There is good reason to suspect a detrimental effect of helminth infection on the course of
HIV infection. We hypothesize, that treatment of helminths in HIV- and helminth co-infected
individuals leads to a reduction of HIV viral load. With a lower HIV RNA level one would
expect a slower decline of CD4 cells and hence also a slower progression of the disease.
Ideally this would lead to a prolongation of the chronic phase of HIV infection and to a
delay in the time when anti-retroviral treatment needs to be started.
* Background: On the basis of immunological considerations and in vitro trials on
co-infections there is strong reason to suspect a detrimental effect of helminth infection
on the course of HIV. The immunological answer very efficiently evoked by helminth infection
is aimed at hijacking and suppressing the immune system in order to suit the requirements of
the specific helminth. This permits helminths to cause chronic infection, often persisting
over years and allowing some infecting worms to grow to several centimetres of length within
their host. However, this immune modulation also affects non-related antigens (for example
HIV) which would actually require a different line of immunological action.
Some clinical trials have been able to confirm this detrimental effect of helminths on HIV
infection, while other trials failed to do so. A recent Cochrane review on clinical trials
with HIV and helminth co-infection found an overall slight reduction of HIV viral load if
helminth infection was treated. However there was no measurable effect on CD4 count or
clinical staging of HIV. This might be explained by the fact that these trials were very
heterogeneous in their set-up and were run for too short a time (max 6 months) to allow
sufficient answers to these questions.
According to mathematical models, even a relatively modest reduction of HIV RNA by 0.5 log
could delay the need to start combined antiretroviral therapy by about 3.5 years and
potentially prolong the symptom-free phase of HIV-infection by nearly 1 year. On a
population scale this could lead to substantial savings with regard to drug and clinical
costs and on an individual level to an invaluable gain in drug-free and ideally also
symptom-free life years.
- Objective: To assess the impact of presumptive anthelminthic treatment on HIV
progression in patients infected with HIV in a rural setting with presumed high
prevalence of helminth infection.
- Methods: Randomised open-label trial of presumptive triple anthelminthic treatment in
HIV positive patients not yet requiring anti-retroviral treatment.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05454514 -
Automated Medication Platform With Video Observation and Facial Recognition to Improve Adherence to Antiretroviral Therapy in Patients With HIV/AIDS
|
N/A | |
Completed |
NCT03760458 -
The Pharmacokinetics, Safety, and Tolerability of Abacavir/Dolutegravir/Lamivudine Dispersible and Immediate Release Tablets in HIV-1-Infected Children Less Than 12 Years of Age
|
Phase 1/Phase 2 | |
Completed |
NCT03141918 -
Effect of Supplementation of Bioactive Compounds on the Energy Metabolism of People Living With HIV / AIDS
|
N/A | |
Completed |
NCT03067285 -
A Phase IV, Open-label, Randomised, Pilot Clinical Trial Designed to Evaluate the Potential Neurotoxicity of Dolutegravir/Lamivudine/Abacavir in Neurosymptomatic HIV Patients and Its Reversibility After Switching to Elvitegravir/Cobicistat/Emtricitabine/Tenofovir Alafenamide. DREAM Study
|
Phase 4 | |
Recruiting |
NCT04579146 -
Coronary Artery Disease (CAD) in Patients HIV-infected
|
||
Completed |
NCT06212531 -
Papuan Indigenous Model of Male Circumcision
|
N/A | |
Active, not recruiting |
NCT03256422 -
Antiretroviral Treatment Taken 4 Days Per Week Versus Continuous Therapy 7/7 Days Per Week in HIV-1 Infected Patients
|
Phase 3 | |
Completed |
NCT03256435 -
Retention in PrEP Care for African American MSM in Mississippi
|
N/A | |
Completed |
NCT00517803 -
Micronutrient Supplemented Probiotic Yogurt for HIV/AIDS and Other Immunodeficiencies
|
N/A | |
Active, not recruiting |
NCT03572335 -
Systems Biology of Diffusion Impairment in Human Immunodeficiency Virus (HIV)
|
||
Completed |
NCT04165200 -
Fecal Microbiota Transplantation as a Therapeutic Strategy for Patients Infected With HIV
|
N/A | |
Recruiting |
NCT03854630 -
Hepatitis B Virus Vaccination in HIV-positive Patients and Individuals at High Risk for HIV Infection
|
Phase 4 | |
Terminated |
NCT03275571 -
HIV, Computerized Depression Therapy & Cognition
|
N/A | |
Completed |
NCT02234882 -
Study on Pharmacokinetics
|
Phase 1 | |
Completed |
NCT01618305 -
Evaluating the Response to Two Antiretroviral Medication Regimens in HIV-Infected Pregnant Women, Who Begin Antiretroviral Therapy Between 20 and 36 Weeks of Pregnancy, for the Prevention of Mother-to-Child Transmission
|
Phase 4 | |
Recruiting |
NCT05043129 -
Safety and Immune Response of COVID-19 Vaccination in Patients With HIV Infection
|
||
Not yet recruiting |
NCT05536466 -
The Influence of Having Bariatric Surgery on the Pharmacokinetics, Safety and Efficacy of the Novel Non-nucleoside Reverse Transcriptase Inhibitor Doravirine
|
N/A | |
Recruiting |
NCT04985760 -
Evaluation of Trimer 4571 Therapeutic Vaccination in Adults Living With HIV on Suppressive Antiretroviral Therapy
|
Phase 1 | |
Completed |
NCT05916989 -
Stimulant Use and Methylation in HIV
|
||
Terminated |
NCT02116660 -
Evaluation of Renal Function, Efficacy, and Safety When Switching From Tenofovir/Emtricitabine Plus a Protease Inhibitor/Ritonavir, to a Combination of Raltegravir (MK-0518) Plus Nevirapine Plus Lamivudine in HIV-1 Participants With Suppressed Viremia and Impaired Renal Function (MK-0518-284)
|
Phase 2 |