跳至主要内容
临床试验/NCT04947176
NCT04947176进行中(未招募)不适用

A Double Blind, Randomized, Single Center, Controlled, Two Arm Trial of Dietary C15:0 Supplementation in Young Adults at Risk for Metabolic Syndrome

Jeffrey B. Schwimmer, MD2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2021年7月6日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
30
试验地点
2
主要终点
Change in plasma C15:0 levels

研究概览

简要总结

This study will determine changes in plasma C15:0 levels in young adults with BMI ≥ 25 in response to 12 weeks of daily oral C15:0 supplementation.

详细描述

Metabolic syndrome is a disturbance in how the body processes both carbohydrates and fats. This condition has become common in children and young adults, especially in association with excess body fat. People with metabolic syndrome are at increased risk for type 2 diabetes, cardiovascular disease, and nonalcoholic fatty liver disease (NAFLD). Diet is believed to play an important role in both developing and treating metabolic syndrome. Studies have shown that low dietary intake of a type of fats known as odd chain fatty acids is associated with a higher risk for each of the metabolic syndrome associated conditions of diabetes, heart disease, and liver disease. Supplementation with one specific odd chain fatty acid known as C15:0 has shown to decrease the effects of metabolic syndrome in both cellular and animal models. In people, the epidemiology of consumption of C15:0 in the diet is consistent with this belief. However, clinical trials have yet to be done with supplemental C15:0. This study is a pilot study of C15:0 supplementation in a group of young adults at risk for metabolic syndrome. The study will determine how well supplementation with C15:0 daily for 12 weeks is able to raise levels of C15:0 in the blood when compared to placebo. The study will also look for signs that increasing blood levels of C15:0 leads to changes in physiology.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 through 25 years
  • Body Mass Index ≥ 25 Kg/m2

排除标准

  • Reported habitual dietary intake of C15:0 that consistently exceeds 250 mg per day
  • Significant alcohol consumption (average consumption >1 drink/day for females, >2 drink/day for males or episodes of binge drinking >5 drinks/day)
  • Inability to swallow capsules
  • Type 1 or Type 2 Diabetes
  • Liver Cirrhosis
  • Pregnancy
  • Body weight greater than 125 kg at screening
  • LDL-cholesterol > 160 mg/dL
  • Triglycerides > 500 mg/dL
  • Hemoglobin < 10.0 gm/dL
  • Current Omega 3 Fatty Acid supplement usage
  • Current use of Statin medications
  • Any other condition which, in the opinion of the investigator, would impede compliance or hinder completion of the study
  • Patients who are currently enrolled in a clinical trial or who received an investigational study drug within 180 days of screening.
  • Subjects who are not able or willing to comply with the protocol or have any other condition that would impede compliance or hinder completion of the study, in the opinion of the investigator.
  • Failure to give informed consent

结局指标

主要结局

Change in plasma C15:0 levels

时间窗: Baseline to 12 weeks

To determine changes in plasma C15:0 levels in response to daily supplementation of C15:

次要结局

  • Change in hemoglobin(Baseline to 12 weeks)
  • Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability](Baseline to 12 weeks)
  • Change in serum glutamyl transpeptidase(Baseline to 12 weeks)
  • Change in BMI(Baseline to 12 weeks)
  • Change in serum alanine aminotransferase(Baseline to 12 weeks)
  • Change in serum aspartate aminotransferase(Baseline to 12 weeks)
  • Change in Weight(Baseline to 12 weeks)
  • Change in serum LDL-cholesterol(Baseline to 12 weeks)
  • Change in serum HDL-cholesterol(Baseline to 12 weeks)
  • Change in High Sensitivity C-reactive protein(Baseline to 12 weeks)
  • Change in serum glucose(Baseline to 12 weeks)
  • Change in serum insulin(Baseline to 12 weeks)
  • Change in serum total cholesterol(Baseline to 12 weeks)

研究者

发起方
Jeffrey B. Schwimmer, MD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jeffrey B. Schwimmer, MD

Professor

University of California, San Diego

研究点 (2)

Loading locations...

相似试验