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Starting soon Observational

Inflammation and Diabetes: Evaluating Antioxidant Levels

NCT07734428 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-07-15
Last updated
2026-07-29

Condition(s) studied

Diabete MellitusDiabete Type 2InflamationSystemic InflammationDietary Inflammatory Index (DII)Systemic Inflammation Markers

Investigational drug(s) / intervention(s)

No Interventions

No Interventions: No interventions

Study summary

The goal of this observational, cross-sectional study is to evaluate the relationships between dietary total antioxidant capacity, systemic inflammatory response markers, and nutritional parameters in adult patients with Type 2 Diabetes (T2DM). Participants will be classified into controlled (HbA1c \< %7) and uncontrolled (HbA1c ≥ %7) diabetes groups based on their glycemic control. The main questions it aims to answer are: Does dietary antioxidant capacity affect systemic inflammation levels and metabolic parameters? Is there a relationship between nutritional risk status and inflammatory response in T2DM patients?

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18 and older diagnosed with Type 2 Diabetes. * Individuals whose biochemical analyses have been performed by a physician within the last 1 month. * Individuals willing to participate voluntarily. Exclusion Criteria: * Missing required laboratory data in the last 1 month. * Presence of acute infection or inflammatory disease. * Advanced kidney or liver failure. * Active malignancy or receiving chemotherapy/radiotherapy. * Pregnant and lactating women. * Use of antioxidant/vitamin-mineral supplements. * Receiving special diet therapies (e.g., time-restricted, ketogenic, or elimination diet). * Advanced cognitive impairment or communication difficulties.

Primary outcome measure(s)

  • Composite Dietary Antioxidant Index (CDAI) — Baseline
    The Composite Dietary Antioxidant Index (CDAI) will be calculated to evaluate the total and synergistic effect of dietary antioxidants. It is based on the standardized daily intake of six main antioxidant components: Vitamin A, Vitamin C, Vitamin E, Magnesium, Selenium, and Zinc. Nutrient data will be obtained from food consumption records using the BeBiS 9 nutritional software. For each antioxidant nutrient, a unitless Z-score will be calculated by subtracting the population's mean intake from the individual's intake and dividing by the standard deviation.
  • The Dietary Antioxidant Index — Baseline
    The Dietary Antioxidant Index (DAI) will be calculated based on the daily antioxidant intake obtained from the participants' food frequency questionnaire data. The main dietary antioxidant components (Vitamin C, Vitamin E, $\\beta$-carotene, flavonoids, and other polyphenols) will be quantitatively determined using the BeBiS 9 nutritional software. For each antioxidant component, the obtained values will be standardized into a Z-score by subtracting the mean intake of the study population from the individual's intake and dividing by the standard deviation. The individual's final DAI score will then be calculated by summing the Z-scores of all these components.
  • Systemic Immune-Inflammation Index (SII) — Baseline
    Calculated from peripheral blood parameters using the formula: Platelet count × Neutrophil count / Lymphocyte count.
  • Systemic Inflammation Response Index (SIRI) — Baseline
    Calculated using the formula: Neutrophil count × Monocyte count / Lymphocyte count.
  • Triglyceride-Glucose (TyG) Index — Baseline
    Calculated using fasting plasma glucose and fasting triglyceride levels as an indirect marker of insulin resistance.
  • Nutritional Assessment - Nutritional Risk Screening 2002 (NRS-2002) — Baseline
    The nutritional risk of the participants will be evaluated using the Nutritional Risk Screening 2002 (NRS-2002) tool. The NRS-2002 assesses impaired nutritional status and disease severity. The total score ranges from 0 to 7. A total score of 3 or higher indicates that the patient is at nutritional risk, while a score less than 3 indicates no immediate nutritional risk. The assessment will be administered by the researcher at the beginning of the study.
  • Nutritional Assessment - Malnutrition Universal Screening Tool (MUST) — Baseline
    The nutritional risk of the participants will be evaluated using the Malnutrition Universal Screening Tool (MUST). MUST is a validated screening tool used to identify adults who are malnourished or at risk of malnutrition. The score is calculated based on three parameters: current body mass index (BMI), unintentional weight loss, and the effect of acute disease. The total score ranges from 0 to 6. A score of 0 indicates low risk, a score of 1 indicates medium risk, and a score of 2 or higher indicates a high risk of malnutrition. The assessment will be administered by the researcher at the beginning of the study.

Trial sites (1)

FacilityCityRegionStatus
Gaziosmanpasa Training and Research Hospital Istanbul Turkey (Türkiye)
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07734428 on ClinicalTrials.gov ↗ ← All trials in Turkey