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Active Hexose Correlated Compound in Tuberculosis-HIV (Human Immunodeficiency Virus) Infection

Effect of Active Hexose Correlated Compound to Clinical and Immunological Response in Tuberculosis-HIV (Human Immunodeficiency Virus) Infection

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05100758
Enrollment
120
Registered
2021-10-29
Start date
2018-10-01
Completion date
2020-12-01
Last updated
2021-10-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Human Immunodeficiency Virus, Tuberculosis

Keywords

Active Hexose Correlated Compound, Tuberculosis-HIV, Cytokine, Sputum Conversion

Brief summary

Background Active Hexose Correlated Compound is assumed to have a positive effect on immunity, including induce a phagocytic response, reduce tumor resistance, and cytokine response including interferon-gamma and interleukins. Tuberculosis patients with concurrent Human immunodeficiency Virus (HIV) might have benefit when receiving active hexose compound during tuberculosis treatment Purposes 1. To assess the clinical changes of patients who receive active hexose compound as an adjuvant to tuberculosis therapy in patients with HIV 2. To assess the difference of pro-inflammatory cytokines between standard therapy and active hexose compound adjuvant Methods A clinical trial involving patients with Tuberculosis-HIV infection Hypothesis 1. Clinical improvement is significantly different where the group who receive active compound will have the better clinical outcome 2. Lower proinflammatory cytokines are observed in people who receive active compound

Detailed description

Population : Lung Tuberculosis patient with HIV Infection Design : Double-Blind Randomized Control Trial at the outpatient setting Randomization Simple Randomization Proposed Number of participants : Using the difference between two independent means of duration to sputum conversion 1. Type 1 error 5% 2. Power of study 80% 3. Effect Size 0.5 4. Dropout rate 20% Total Participant 122 Proposed analysis 1. Time-to-event analysis using cox regression for the duration of sputum conversion and radiology resolution 2. Linear mixed model for continuous dependent variable

Interventions

DIETARY_SUPPLEMENTActive Hexoses Correlated Compound

Active Hexose Correlated Compound was isolated from basidiomycetes which comprise polysaccharides and amino acids.

Sponsors

Hasanuddin University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

Investigator will be blinded from the allocation (not allowed to observe the allocation and intervention) and the outcome assessor will not be informed the code of allocation

Intervention model description

One group will be given Active Hexose Correlated Compound as adjuvant and the comparison group will only receive the tuberculosis treatment

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Newly-diagnosed Lung Tuberculosis case who will receive a 6-month regiment 2. Not Pregnant 3. Diagnosed with HIV

Exclusion criteria

1. Patient with liver dysfunction 2. Patient with drug-resistant 3. Severe Malnutrition 4. Refuse to be involved

Design outcomes

Primary

MeasureTime frameDescription
Sputum Conversion Durationsix month after the intervention startedSputum conversion duration defined as the duration to change positive result in sputum smear into negative results. The sputum smear level using Ziehl Neelsen ranging from Negative to 3+.
Chest X-Ray ExtensionChanges of number of active tuberculosis feature from baseline to 6 monthsDistribution of active tuberculosis feature in Chest X-Ray including number of consolidation and cavitation
Interleukin 6 LevelChanges of Interleukin 6 Level from baseline to 6 monthsValue of Interleukin 6 in blood Sample
Interleukin 10 LevelChanges of Interleukin 10 value from baseline to 6 monthsValue of Interleukin 10 in blood Sample

Secondary

MeasureTime frameDescription
Cluster Differentiation 4 (CD4) cells valueChanges of Cluster Differentiation 4 (CD4) cells value from baseline to 6 monthsCluster Differentiation 4 (CD4) cells value in blood sample
Cluster Differentiation 8 (CD8) cells valueChanges of Cluster Differentiation 8 (CD8) cells value from baseline to 6 monthsCluster Differentiation 8 (CD8) cells value in blood sample

Countries

Indonesia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026