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临床试验/NCT03902301
NCT03902301已完成不适用

The Effect of Lactobacillus Rhamnosus Supplementation on Body Mass, Hyperandrogenism and Insulin Resistance in Overweight and Obese Polycystic Ovary Syndrome Women - Randomized Nutritional Study

Poznan University of Life Sciences2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2018年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
80
试验地点
2
主要终点
Testosterone

研究概览

简要总结

The effect of Lactobacillus rhamnosus supplementation on body weight, hyperandrogenism and insulin resistance in overweight and obesity women with Polycystic Ovary Syndrome will be analysed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Investigator)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • patients diagnosed with PCOS,
  • BMI> 28 kg/m2 (overweight or obesity),
  • patients not participating in other similar research programs at the same time,
  • no previous operations on ovaries such as: laparoscopy, ovarian cautery etc.,
  • written agreement to take part in the research.
  • Exlusion criteria:
  • the use of antibiotics or probiotics within 6 months before the start of the experiment,
  • the use of pharmacological agents or hormones that may affect the course of the menstrual cycle or metabolic rate within 3 months,
  • the use of medicament that may affect on carbohydrate metabolism within 4 weeks,
  • failure to comply with dietary recommendations established during the nutritional intervention,
  • the use of weight loss supplements during the study,
  • clinical diagnosis of digestive disease (for example: irritable bowel syndrome, ulcerative colitis, Crohn's disease, celiac disease),
  • pregnancy and breast feeding.

排除标准

  • 未提供

结局指标

主要结局

Testosterone

时间窗: 20 weeks

Testosterone (ng/mL) concentrations will measured at baseline and after 20 weeks of the intervention. Results of testosterone level and SHBG level will be combined to report FAI index (index of free androgen).

SHBG

时间窗: 20 weeks

SHBG (nmol/L) concentrations will measured at baseline and after 20 weeks of the intervention. Results of testosterone level and SHBG level will be combined to report FAI index (index of free androgen).

Body composition

时间窗: 20 weeks

Fat mass (%), fat free mass (%) will be assessment at baseline and after 20 weeks of the intervention.

Blood lipid profile: cholesterole

时间窗: 20 weeks

Cholesterole (mg/dL) will be measured at baseline and after 20 weeks of the intervention

Blood lipid profile: low density lipoprotein

时间窗: 20 weeks

Low density lipoprotein LDL (mg/dL) will be measured at baseline and after 20 weeks of the intervention

Insulin Resistance

时间窗: 20 weeks

Fasting insulin concentration (uU/ml) will be measured before and after 2 hours of 75g glucose drink. Insulin resistance will be measured before and after 20 weeks of the intervention.

Oral glucose test OGTT

时间窗: 20 weeks

Fasting glucose concentration (mg/dL) will be measured before and after 2 hours of 75g glucose drink. OGTT will be measured before and after 20 weeks of the intervention. Fating glucose and fasting insulin concentrations will be combined to report HOMA-IR index (homeostatic model assessment of insulin resistance).

DHEA-SO4

时间窗: 20 weeks

DHEA-SO4 (umol/L) concentrations will measured at baseline and after 20 weeks of the intervention. Results of testosterone level and SHBG level will be combined to report FAI index (index of free androgen).

Free androgen index FAI

时间窗: 20 weeks

Results of testosterone level and SHBG level will be combined to report FAI index (index of free androgen).

Blood lipid profile: triglicerydes

时间窗: 20 weeks

Triglicerydes (mg/dL) will be measured at baseline and after 20 weeks of the intervention

Body height

时间窗: Baseline

Body height (cm) will be assessment at baseline of the intervention.

Body weight

时间窗: 20 weeks

Body weight (kg) will be assessment at baseline and after 20 weeks of the intervention.

Blood lipid profile: high density lipoprotein

时间窗: 20 weeks

High density lipoprotein HDL (mg/dL) will be measured at baseline and after 20 weeks of the intervention

次要结局

  • Assessment of qualitative and quantitative of the microbiome(20 weeks)
  • Assessment of B-glucuronidase and B-glucosiadase activity(20 weeks)
  • Assessment of short-chain fatty acids(20 weeks)

研究者

发起方
Poznan University of Life Sciences
申办方类型
Other
责任方
Principal Investigator
主要研究者

Karolina Łagowska

Principal Investigator (dr inż)

Poznan University of Life Sciences

研究点 (2)

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