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OpenTrials
Completed

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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Key information

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

PMT25341

Dietary Supplement

Placebo

Dietary Supplement

Lactose

Primary outcomes

  1. Safety and tolerability: Number of participants with treatment-related adverse events as assessed by CTCAE v4.0

    Time frame: From baseline through week 48

  2. Changes in CD4+ T cell counts/uL

    Time frame: From baseline through week 48

  3. Changes in CD8+ T cell counts/uL

    Time frame: From baseline through week 48

  4. Changes in CD4/CD8 ratio

    Time frame: From baseline through week 48

Secondary outcomes

  1. Microbiota composition: alpha-diversity

    Time frame: From baseline through week 48

  2. Microbiota composition: Unifrac distances

    Time frame: From baseline through week 48

  3. Microbiota composition: Canberra distances

    Time frame: From baseline through week 48

  4. Changes in plasma soluble CD14 levels

    Time frame: From baseline through week 48

  5. Changes in plasma hs-CRP levels

    Time frame: From baseline through week 48

  6. Changes in plasma IFABP levels

    Time frame: From baseline through week 48

  7. Changes in plasma lipoteichoic acid levels

    Time frame: From baseline through week 48

  8. Changes in plasma kynurenine/tryptophan ratio

    Time frame: From baseline through week 48

  9. 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.