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临床试验/NCT05949008
NCT05949008进行中(未招募)4 期

Effect of Metformin ER With Hypocaloric Diet on Weight Loss in Overweight/Obese Patients With Increased Waist Circumference

University of California, Los Angeles2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2023年11月22日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
进行中(未招募)
入组人数
150
试验地点
2
主要终点
Number of participants who achieve body weight reduction ≥5% from baseline

研究概览

简要总结

Metformin is a drug used to treat patients with diabetes. The aim of this study is to examine the effect of Metformin along with a low-calorie diet on obese and/or overweight adults with an increased waist measurement. In addition, the study also aims to look at the effect of the drug vs. placebo on quality of life and physical activity.

详细描述

Obesity is a growing epidemic in the United States. Weight gain is associated with an increased risk of developing life-threatening conditions such as high blood pressure or diabetes. Therefore, there is great interest in developing non-invasive treatments to help combat obesity. Currently, there are only few weight-loss drugs available for the treatment of obesity. In the more recent past, GLP-1 analogues (a type of non-insulin medication used to treat patients with diabetes) are being promoted as a new strategy to lose weight without major side effects however, with high costs and challenging supply chain issues.

This is a double-blinded, randomized study. This means that participants will be assigned to one of two groups. Participants will have a 1:1 chance of being assigned to receive either the study drug or a placebo (a capsule that does not contain the active ingredients). This assignment will be determined by chance. The process is similar to drawing cards or picking straws. This means your assignment to one of the groups is based on chance and not a medical decision made by the study doctor. In addition, neither participants nor the investigators will know what groups participants have been assigned to.

During this study, your participation will last up to 26 weeks (including screen) with a total of 8 clinic visits. Participants will undergo a total of 5 blood draws, blood samples will be taken at screen baseline and weeks 8, 16 and 24.

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
Double (Participant, Investigator)

入排标准

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

入选标准

  • Male or female, age ≥ 18 years at the time of signing informed consent.
  • Body Mass Index (BMI) ≥ 27 kg/m2
  • Waist circumference >40" for men, and >35" for women

排除标准

  • A self-reported change in body weight > 5 kg (11 lbs) within 90 days before screening irrespective of medical records
  • Diagnosed with T2D (HbA1c >7.5 (53 mmol/mol)
  • Current use of insulin or oral medication of metformin, SU, SGLT2i, glitazone, DPP4 or GLP-1 agonist injections as single agent therapy or combination oral agents.
  • Renal impairment measured as estimated Glomerular Filtration Rate (eGFR) value of < 45 mL/min/1.73 m2 (< 60 ml/min/1.73 m2 in subjects treated with SGLT2i) according to CKDEPI creatinine equation as defined by KDIGO 201242 by the central laboratory at screening
  • History of thyroid disease, but not taking medication or medication dosage changed one or more times over last 6 months (History of thyroid disease and on a stable dose of prescription medication for 6 months or longer is acceptable).
  • History or lactic acidosis
  • Liver problems
  • Congestive heart failure
  • History of alcoholism
  • Recent surgery
  • Heart attack, severe infection or stroke
  • Any unstable medical conditions or terminal diagnosis
  • Pregnancy or lactation
  • Allergy and intolerance to metformin

研究组 & 干预措施

Metformin Extended Release (ER) Oral Tablets

Experimental

This is a 24-week, randomized, double-blinded, two arm parallel clinical trial comparing metformin ER vs. placebo in combination with a hypocaloric diet (-500 kcal/day). 150 individuals with obesity and increased waist circumference will be randomized to taking metformin ER with hypocaloric diet or placebo with hypocaloric diet. All patients will receive dietary and exercise counseling with the intent of reducing their average caloric intake by 500 kcal/day.

干预措施: Metformin Extended Release (ER) Oral Tablet (Drug)

Placebo

Placebo Comparator

Patients in the placebo arm will be randomized to placebo with hypocaloric diet. All patients will receive dietary and exercise counseling with the intent of reducing their average caloric intake by 500 kcal/day.

干预措施: Placebo (Drug)

结局指标

主要结局

Number of participants who achieve body weight reduction ≥5% from baseline

时间窗: 24 Weeks

Percent change in body weight reduction ≥5% from baseline (week 0) to week 24.

Change in total body weight from baseline

时间窗: 24 Weeks

Percent change in total body weight (TBW) from baseline (week 0) to week 24 in body weight.

次要结局

  • Change in total Body Mass Index (BMI) from baseline(24 Weeks)
  • Change in waist circumference from baseline(24 weeks)
  • Percent change in body composition from baseline(24 weeks)
  • Change in insulin sensitivity from baseline(24 Weeks)
  • Change in fasting blood lipids from baseline(24 Weeks)
  • Change in vascular function parameters (blood pressure and pulse wave velocity)(24 weeks)
  • Change in inflammatory markers from baseline(24 weeks)
  • Change in daily dietary intake (calories and macronutrients)(24 weeks)
  • Change in physical activity levels from baseline(24 weeks)
  • Change in quality of life from baseline(24 weeks)
  • Change in glycemic control(24 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Vijaya Surampudi MD

Principal Investigator

University of California, Los Angeles

研究点 (2)

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