NCT Number: NCT03009032
Synbiotics in Advanced HIV Infection
Late diagnosed HIV-infected subjects show impaired immunological recovery resulting in a greater risk of clinical progression. Gut bacteria metabolism appears to impact immune recovery in HIV-infected subjects, and while nutritional interventions with prebiotics and probiotics seem to exert immunological effects, the clinical implications in this key population remain unknown. This is a pilot multicenter randomized placebo-controlled, double blind clinical trial in HIV-infected ART-naive subjects with <350 CD4 T cells/mm3 or AIDS. Participants will be randomized (1:1) to either the synbiotic nutritional supplement PMT25341 or placebo for 48 weeks, each in combination with first-line ART. Primary outcomes will be safety and immunological recovery. Secondary outcomes will include changes in fecal microbiota structure and plasma inflammatory markers.
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Notify MeKey information
Conditions
Age range
18 year–80 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- HIV-infected ART-naive subjects with <350 CD4 T cells/mm3 or AIDS
- Initiating ART with any first-line regimen recommended in the Spanish GESIDA National Guidelines
Exclusion criteria
- Age <18 years
- Pregnancy
- Type 1 or 2 diabetes
- End-stage renal disease
- Lactose intolerance
- Use of immunomodulatory drugs
- Neutrophil count <750cells/uL
Treatment and study plan
Placebo
Dietary SupplementLactose
Primary outcomes
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Safety and tolerability: Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Time frame: From baseline through week 48
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Changes in CD4+ T cell counts/uL
Time frame: From baseline through week 48
-
Changes in CD8+ T cell counts/uL
Time frame: From baseline through week 48
-
Changes in CD4/CD8 ratio
Time frame: From baseline through week 48
Secondary outcomes
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Microbiota composition: alpha-diversity
Time frame: From baseline through week 48
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Microbiota composition: Unifrac distances
Time frame: From baseline through week 48
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Microbiota composition: Canberra distances
Time frame: From baseline through week 48
-
Changes in plasma soluble CD14 levels
Time frame: From baseline through week 48
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Changes in plasma hs-CRP levels
Time frame: From baseline through week 48
-
Changes in plasma IFABP levels
Time frame: From baseline through week 48
-
Changes in plasma lipoteichoic acid levels
Time frame: From baseline through week 48
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Changes in plasma kynurenine/tryptophan ratio
Time frame: From baseline through week 48
-
Changes in percentage of HLADR+/CD38+ T cells
Time frame: From baseline through week 48
Sponsors and collaborators
Lead sponsor
Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal
Other
Collaborators
- Hospital San Carlos, Madrid
- Hospital San Pedro de Logroño
- Hospital Universitario 12 de Octubre
- Hospital Universitario La Paz
- Hospital del Mar
- Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz
Registry information
Official study title
Immunological Effects of an Immunomodulatory Synbiotic Intervention at Advanced HIV Disease
Acronym: PROMALTIA
Important dates
- Study start
- 2014
- Primary completion
- 2017
- Study completion
- 2017
- First posted
- Jan 4, 2017
- Registry last updated
- Aug 1, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.