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临床试验/NCT01981343
NCT01981343已完成2 期

A Randomized, Double Blind, Placebo Controlled Parallel Study Evaluating the Effect of A-F Betafood® on Gallbladder and Liver Function.

KGK Science Inc.2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2013年11月11日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
50
试验地点
2
主要终点
Gallbladder and Liver function

研究概览

简要总结

Gallstone formation is multifactorial: immutable risk factors include genetics and ethnicity, age and being female, and mutable risk factors include obesity, and metabolic syndrome, diet, rapid weight loss, and other conditions such as cirrhosis, Crohn's disease, irritable bowel syndrome, gallbladder stasis, and the use of certain drugs like Ceftriazone. Previous studies have linked serum cholesterol, and low-density lipoprotein cholesterol levels and fatty liver disease to gallbladder disease. Given betaine's reported beneficial effects on fatty liver and lipid profile, A-F Betafood® may have a beneficial effect on gallbladder function.

The objective of the study is to assess the effect of A-F Betafood® on gallbladder and liver function as measured by gallbladder ultrasounds and liver function tests. The hypothesis is that A-F Betafood® will improve gallbladder and liver function after the 12 week treatment period.

This is a single-center, randomized, double-blind, placebo-controlled, parallel group study with two arms. This study will consist of a single 12 week treatment period. The planned sample size for this study is 50 overweight female subjects, with 25 subjects randomized equally to each of the two study arms in double-blind manner at a ratio of 1:1

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
40 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Females 40-75 years of age or older not of child bearing potential. Defined as females who have had a hysterectomy or oophorectomy, bilateral tubal ligation or are post-menopausal (natural or surgically with > 1 year since last menstruation).OR Female subject of childbearing potential must agree to use a medically approved method of birth control and have a negative urine pregnancy test result
  • BMI of 25.0 kg/m2 to 29.9 kg/m2
  • Agrees to comply with study procedures
  • Healthy as determined by laboratory results, medical history and physical exam
  • Has given voluntary, written, informed consent to participate in the study
  • Gastrointestinal distress with various fatty foods as determined by the modified GSRS questionnaire
  • Family history of gallbladder disease or previous history of gallbladder attacks
  • Has a normal resting heart rate 50-80bpm

排除标准

  • Women who are pregnant, breastfeeding, or planning to become pregnant during the course of the trial
  • Unstable psychiatric disorder requiring hospitalization within past 6 months
  • Use of prescription medications, over the counter medications or natural health products/dietary supplements known to affect gastric/gastrointestinal function within 4 weeks of randomization
  • Presence of gallstones as determined by ultrasound
  • Uncontrolled hypertension defined as untreated systolic blood pressure > 160 mmHg and/or diastolic blood pressure > 100 mmHg
  • Clinically significant abnormal laboratory results at screening including: AST, ALT and/or bilirubin > 2 x the ULN; Serum creatinine >1.5 x the ULN or eGFR < 60; Hemoglobin < 123 g/L
  • Participation in a clinical research trial within 30 days prior to randomization
  • Allergy or sensitivity to test article ingredients, soy, dairy, egg, wheat, peanut, tree nuts, fish or shellfish.
  • Individuals who are cognitively impaired and/or who are unable to give informed consent
  • Any other condition which in the Investigator's opinion may adversely affect the subject's ability to complete the study or its measures or which may pose significant risk to the subject

研究组 & 干预措施

A-F Betafood

Experimental

Two A-F Betafood tablets taken with a meal, 3 times daily for 12 weeks

干预措施: A-F Betafood (Dietary Supplement)

Placebo

Placebo Comparator

2 Placebo tablets taken with a meal, 3 times daily for 12 weeks

干预措施: Placebo (Other)

结局指标

主要结局

Gallbladder and Liver function

时间窗: 12 weeks

Changes in Gallbladder Ultrasound and Liver function tests (fasting serum AST, ALT, GGT and hsCRP)

次要结局

  • Fasting Oxidized LDL(12 weeks)
  • Fasting TNF-alpha(12 weeks)
  • Heart Rate(Over 12 weeks)
  • Adverse events(Over 12 weeks)
  • Gastrointestinal distress(12 weeks)
  • Fasting Lipid Profile(12 weeks)
  • Blood Pressure(Over 12 weeks)
  • Blood Safety Parameters(Over 12 weeks)
  • Fasting Adiponectin(12 weeks)
  • Biometrics: weight and BMI(Over 12 weeks)
  • Fasting Malonyldialdehyde(12 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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