Intestinal Endotoxemia and Beta- Cell Dysfunction in Prediabetics

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorSohag University

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 volunteers

Qualifiers

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

Design model

Case-control

Time perspective

Cross-sectional

Treatments tested in this trial

  • hba1c, lbp, fasting blood sugar, lipogram, fastinf insulin

    Diagnostic test

    diagnostic tests for prediabetes and intestinal endotoxemia

Treatment groups

120 Participants
are divided into 2 treatment groups
Group A: group 1: cases1 intervention
Group B: group 2:controls1 intervention

Trial outcomes

Primary outcomes

1

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).

Time frame
one year

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: