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Effect of probiotics on patients with type 2 diabetes

Effect of probiotics on lipid profile, glycemic control and insulin levels, oxidative stress and inflammatory parameters in patients with type 2 diabetes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201109197598N1
Enrollment
40
Registered
2011-10-07
Start date
2010-09-06
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Type 2 Diabetes. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: Intervention: patients in the treatment group received 1500 mg probiotic capsules twice daily (after lunch and dinner meals) for 6 weeks. The lactobacillus Probiotics contain: L. acid
Treatment - Drugs
Placebo
Control: Placebo Group receiving 1500 mg Magnesium Stearate capsules twice daily, for six weeks.
Intervention: patients in the treatment group received 1500 mg probiotic capsules twice daily (after lunch and dinner meals) for 6 weeks. The lactobacillus Probiotics contain: L. acidophilus

Sponsors

Researches and Technology Deputy of Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Patients with diabetes type 2 were enrolled with FBS = 126 mgr / dl ; less than 15 years of their disease were over ; the age range was 25 to 65 years ; Elective subjects, next drugs prescribed by doctors, should be controlled the status of glucose and lipid levels and during the study could use of these drugs without changing in the prior dosage. Exclusion Criteria: Patients with diabetes type 2 that used replace treatments like Hormone or supplemental vitamin ; Also those used tobacco and alcohol ; patients with chronic kidney disease ; liver ; lung ; chronic or acute inflammatory disease (especially acute pancreatic inflammation and Endocarditis) ; heart valve disease ; short bowel syndrome ; allergies ; people with low immune system ability (autoimmune) ; pregnant or lactating women.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Lipid Profile ( Tg,Total Chol, LDL-C, HDL-C ). Timepoint: Before and After Intervention. Method of measurement: Autoanalyzer.;Serum Glucose. Timepoint: Before and after Intervention. Method of measurement: Autoanalyzer.;Serum Insulin Levels. Timepoint: Before and After Intervention. Method of measurement: ELISA.;Hs-CRP. Timepoint: Before and after intervention. Method of measurement: ELISA.;IL-6. Timepoint: Before and After Intervention. Method of measurement: Autoanalyzer.;Malodialdehyde (MDA). Timepoint: Before and after Intervention. Method of measurement: Specterophotometery.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbbas Yousefinejad

Tehran University of Medical sciences

a-yousefinejad@razi.tums.ac.ir+98 21 6640 2095

Outcome results

None listed

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