Status:
COMPLETED
The Effect of a Multistrain Probiotic on Metformin Tolerance and Efficacy With Microbiota and Stool Metabolome in Insulin-resistant Women - a 12-week Randomized, Placebo-controlled, Double-blind Study
Lead Sponsor:
Poznan University of Physical Education
Conditions:
Insulin Resistance
Eligibility:
FEMALE
25-45 years
Phase:
NA
Brief Summary
The goal of this study is to evaluate the efficacy of metformin on insulin sensitivity and vascular endothelial function with respect to gut microbiota and metabolome in women with established insulin...
Eligibility Criteria
Inclusion
- women 25-45 years old, menstruating, BMI 25-32.9 kg / m2, insulin resistance based on the HOMA-IR index (cut-off point 2.5
Exclusion
- type 1 and 2 diabetes,
- poorly controlled arterial hypertension (mean SBP values\> 140mmHg and / or mean DBP values\> 90mmHg) within the last month and / or the need to modify pharmacological treatment,
- 2nd degree obesity, BMI\> 35 kg / m2,
- lipid disorders requiring pharmacological treatment in the last 3 months before the start of observation or during observation,
- positive history of ischemic heart disease, carotid and / or lower limb atherosclerosis,
- features of heart failure on physical examination and / or additional examinations (chest X-ray, echocardiography),
- clinically significant arrhythmias or conduction disturbances,
- chronic kidney disease with creatinine clearance \<60mL / min / 1.73m2,
- clinically significant impairment of liver function (transaminase values 3 times the normal range),
- acute or chronic, clinically evident inflammatory process (diseases of connective tissue and joints, inflammatory processes of the respiratory tract, inflammatory processes of the genitourinary system, inflammation of the head and neck),
- acute infection in the last month,
- Cancer,
- alcohol abuse, drug addiction,
- taking medications that may interfere with test results,
- Taking antibiotics, steroids, antifungal and antiparasitic agents 4 weeks before the examination (not applicable to topical antifungal agents).
- taking pre - and / or probiotics in the last 12 weeks before the test
- travel to tropical countries in the last 4 weeks prior to the survey
- other conditions that may pose any risk to the patient during the follow-up.
Key Trial Info
Start Date :
April 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 20 2023
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT06092060
Start Date
April 1 2021
End Date
July 20 2023
Last Update
October 23 2023
Active Locations (1)
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1
Poznan University of Physical Education
Poznan, Poland, 61-871