HIV Clinical Trial
Official title:
Diet / Gut Microbiome Interaction and Influence on Inflammatory Disease in HIV Patients
| NCT number | NCT02610374 |
| Other study ID # | 15-1692 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | March 2016 |
| Est. completion date | March 2020 |
| Verified date | January 2022 |
| Source | University of Colorado, Denver |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The primary objective is to assess the effect of short-term diet modification on the microbiome composition, and inflammatory/metabolic disease markers in Antiretroviral therapy (ART)-treated HIV-infected participants and Human immunodeficiency virus (HIV)-negative controls in the United States.
| Status | Completed |
| Enrollment | 90 |
| Est. completion date | March 2020 |
| Est. primary completion date | March 2020 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years to 65 Years |
| Eligibility | Inclusion Criteria: - HIV-infected cohort (Cohort A) - Documentation of HIV-1 infection defined as a positive antibody test or plasma HIV-1 RNA (ribosomal ribonucleic acid). - Treated with ART (minimum of three antiretroviral drugs in regimen) for at least 12 months with no changes in antiretroviral drugs over the past 6 months - Plasma HIV-1 RNA = 50 copies/mL in the preceding 6 months. - HIV-negative cohorts (Cohort B and C) - Documentation of a negative HIV-1 antibody test - All Cohorts - Age 18 to 65 years - Body mass index between 21-29 kg/m2 (non-obese) - Stable weight for at least 3 months (=15% change in body weight) - Negative pregnancy test (if female) Exclusion Criteria: - Use of systemic (oral or parenteral) antibiotics within two months prior to study entry - Active chronic infection such as hepatitis B or C or an active malignancy that requires systemic chemotherapy. |
| Country | Name | City | State |
|---|---|---|---|
| United States | University of Colorado Denver | Aurora | Colorado |
| Lead Sponsor | Collaborator |
|---|---|
| University of Colorado, Denver |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in plasma IL-6 concentration (All Participants) | - The change in plasma IL-6 from baseline to week 4 for all participants (Cohorts A, B & C) assigned to the Agrarian diet group will be compared to participants assigned to the Western diet group. | 4 weeks | |
| Primary | Change in plasma IL-6 concentration (HIV-Infected Participants) | - The change in plasma IL-6 from baseline to week 4 for HIV-infected participants (Cohort A) assigned to an Agrarian diet will be compared to HIV-uninfected participants (Cohort B & C) assigned to an Agrarian diet. | 4 weeks |
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