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Nutraceutical Supplement for Chronic Inflammatory Disorders

Nutraceuticals Supplement for Chronic inflammatory Disorders – Nutrigenomics and Metagenomic Landscape - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075448
Enrollment
40
Registered
2024-10-17
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: E888- Other specified metabolic disorders

Interventions

Intervention1: PolyNutriBio: Dose-1g/day Dose of administration: Oral as capsules Frequency : Daily Duration: Three months Intervention2: Polyherbal Powder: The investigational product, polyherbal po

Sponsors

Department of Health Research Ministry of Health and Family Welfare Government of India
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Individuals with no conventional biomarkers for diabetes, atherosclerosis and arthritis shall be selected from the population belonging to the Thiruvananthapuram district between the age group of 18-60 years after obtaining informed consent. Anthropological data and blood samples shall be collected based on routine laboratory procedure.

Exclusion criteria

Exclusion criteria: Individuals not belonging to the specified age group, without informed consent shall be excluded from the study. Individuals with diagnosed with contagious diseases, chronic illness, cancer or chemotherapy patients shall be excluded from the study. Additionally, pregnant and lactating women shall be excluded from the study.

Design outcomes

Primary

MeasureTime frame
The primary outcome of this study is to assess the efficacy of the nutraceutical mixed polyherbal powder in managing chronic inflammatory disorders. Reductions in the symptoms indicate improvements in disease severity and control, reflecting the effectiveness of the nutraceutical intervention in mitigating chronic inflammation.Timepoint: Baseline and 30, 60, 90 and 120 days

Secondary

MeasureTime frame
To assess anti-inflammatory effect after the trial periodTimepoint: baseline and 30, 60, 90 and 120 days

Countries

India

Contacts

Public ContactDr Maya G Pillai

University of Kerala

helenabios@keralauniversity.ac.in9447399759

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026