About this trial
the goal of this observation study is to learn about association between intestinal endotoxemia and prediabetes lean patients with the aim of prevention of diabetes in those category of patients
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age: 18-65 years
BMI: 18.5-24.9 kg/m²
ADA prediabetes: FPG 100-125 mg/dL OR 2hPG 140-199 mg/dL OR HbA1c 5.7-6.4%
HOMA-IR <1.5 (key inclusion criterion)
Disqualifiers
- HOMA-IR ≥1.5
BMI ≥25 kg/m²
Diabetes, acute inflammation, GI disorders (Table 1) Group II (Controls): Lean normoglycemic ; age and sex-matched healthy subjects
Trial population
The patient population for the trial will be derived from Outpatient clinics, Sohag University Hospital 120 participants .
Trial design
Case-control
Cross-sectional
Treatments tested in this trial
hba1c, lbp, fasting blood sugar, lipogram, fastinf insulin
Diagnostic testdiagnostic tests for prediabetes and intestinal endotoxemia
Treatment groups
Trial outcomes
Primary outcomes
correlation between intestinal endotoxemia (measured by serum LBP) and basal beta-cell dysfunction (HOMA-B) in lean prediabetic patients
To determine the correlation between intestinal endotoxemia (measured by serum LBP) and basal beta-cell dysfunction (HOMA-B) in lean prediabetic patients with minimal insulin resistance (HOMA-IR \<1.5).
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: