Effects of VSL#3 on Neuro-cognitive Profile of HIV Patients
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ClinicalTrials.gov Identifier: NCT02276326 |
Recruitment Status : Unknown
Verified December 2016 by Dott.ssa Gabriella D'Ettorre, Azienda Policlinico Umberto I.
Recruitment status was: Recruiting
First Posted : October 28, 2014
Last Update Posted : June 28, 2018
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Aim of the study is to evaluate the effects of a change in the intestinal microflora on the neuro-cognitive profile of patients with HIV infection receiving HAART treatment. Improvements will be evaluated with questionnaires on Quality of life and Cognitive and Behavior function.
20 patients will be enrolled and will receive 4 sachets of VSL#3 per day.
Condition or disease | Intervention/treatment | Phase |
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HIV Seropositivity ART | Dietary Supplement: VSL#3 sachets | Not Applicable |

Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 20 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Title Effect of Microbial Translocation and Supplementation With the Probiotic VSL#3 on Neuro-cognitive Functions of HIV Positive Patients Receiving HAART |
Study Start Date : | July 2014 |
Estimated Primary Completion Date : | December 2018 |
Estimated Study Completion Date : | June 2019 |
Arm | Intervention/treatment |
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Experimental: VSL#3 sachets
VSL#3 is a mix of lactic acid bacteria and bifidobacteria (original De Simone's formulation)
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Dietary Supplement: VSL#3 sachets
4 sachets a day for 4 months |
- Delta of scores of questionnaires on quality of life [ Time Frame: 4 months ]HIV dementia-scale, Beck Depression Inventory BDI-II, State Trait Anxiety Inventory (STAI Y 1 - Y2), the questionnaire for the assessment of quality of life in persons with HIV infection (ISS-QoL)
- Delta of scores of questionnaires on cognitive functions [ Time Frame: 4 months ]HIV dementia-scale, Beck Depression Inventory BDI-II, State Trait Anxiety Inventory (STAI Y 1 - Y2), the questionnaire for the assessment of quality of life in persons with HIV infection (ISS-QoL)
- Delta of scores of questionnaires on behavioral functions [ Time Frame: 4 months ]HIV dementia-scale, Beck Depression Inventory BDI-II, State Trait Anxiety Inventory (STAI Y 1 - Y2), the questionnaire for the assessment of quality of life in persons with HIV infection (ISS-QoL)
- Delta of value of serum lipopolysaccharide (LPS) [ Time Frame: between time 0 and after 4 months of assumption of VSL#3 ]
- Delta of Cluster of Differentiation 14 (CD14)+ in blood (T0-T1) [ Time Frame: between time 0 and after 4 months of assumption ]
- Delta of value of serum lipopolysaccharide binding protein (LBP) [ Time Frame: between time 0 and after 4 months of assumption ]
- Delta of value of serum EndoCAb [ Time Frame: between time 0 and after 4 months of assumption ]
- Delta of value of serum hs-CRP [ Time Frame: between time 0 and after 4 months of assumption ]
- Delta of value of serum IL-6 [ Time Frame: between time 0 and after 4 months of assumption ]
- Delta of value of serum TNFa [ Time Frame: between time 0 and after 4 months of assumption ]
- Delta of value of serum MIP-lb [ Time Frame: between time 0 and after 4 months of assumption ]

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Men or women at least 18 years of age
- In HAART with HIV RNA <50cp/mL, with CD4 counts> 400 cells / mm
- Availability to release informed consent
Exclusion Criteria:
- Patients with known allergy or intolerance to VSL#3
- Chronic inflammatory bowel diseases
- Drug addiction
- Use of antibiotics or probiotics during the 3 weeks prior the enrollment
- Pregnancy

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02276326
Italy | |
Policlinico Umberto I Hospital | Recruiting |
Rome, Italy, 00155 | |
Contact: Gabriella D'Ettorre gabriella.dettorre@uniroma1.it | |
Principal Investigator: Gabriella D'Ettorre | |
Principal Investigator: Vincenzo Vullo | |
Sub-Investigator: Giancarlo Ceccarelli |
Principal Investigator: | Gabriella D'Ettorre | Policlinico Umberto I Hospital |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | Dott.ssa Gabriella D'Ettorre, PhD, Azienda Policlinico Umberto I |
ClinicalTrials.gov Identifier: | NCT02276326 |
Other Study ID Numbers: |
VSL-Dett 2014 |
First Posted: | October 28, 2014 Key Record Dates |
Last Update Posted: | June 28, 2018 |
Last Verified: | December 2016 |
HIV Seropositivity HIV Infections Lentivirus Infections Retroviridae Infections RNA Virus Infections |
Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases |