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临床试验/NCT07753447
NCT07753447已完成4 期

Calorie Restricted Dietary Intervention in Type 2 Diabetes Patients With Obesity for Remission

Yeouido St. Mary's Hospital1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2025年7月1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
已完成
发起方
入组人数
25
试验地点
1
主要终点
Remission

研究概览

简要总结

This study aims to induce remission of type 2 diabetes through dietary intervention for weight reduction.

详细描述

To promote weight loss, nutritionally balanced low-calorie meal boxes (provided by CJ CheilJedang) will be used. For the purpose of setting an active control group, all participants will also receive Contrave Extended-Release tablets (provided by Kwangdong Pharmaceutical), a medication indicated for weight loss.

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
None

入排标准

年龄范围
19 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Adults aged ≥19 and <60 years
  • Confirmed diagnosis of type 2 diabetes
  • Diagnosed with diabetes within the past 6 years
  • Most recent BMI within the past 3 months ≥27 kg/m²
  • Most recent HbA1c within the past 3 months <11%
  • No insulin therapy within the past 3 months

排除标准

  • Pregnant women or those who may become pregnant during the study period
  • Individuals with organ failure, such as heart failure, hepatic failure, renal failure, or chronic obstructive pulmonary disease
  • History of cardiovascular disease or cancer treatment within the past 6 months
  • Acute illness requiring hospitalization (e.g., infection or surgery) within the past 3 months
  • Presence of endocrine disorders that may affect body weight, such as Cushing's syndrome
  • Use of medications (other than glucose-lowering agents for diabetes) known to affect blood glucose levels within the past 6 months
  • Individuals with known food allergies to specific ingredients in the study meals
  • Individuals with uncontrolled hypertension
  • Individuals with acute alcohol or drug withdrawal symptoms
  • History of seizure disorders such as epilepsy
  • Individuals with genetic disorders such as galactose intolerance, lactase deficiency, or glucose-galactose malabsorption

研究组 & 干预措施

Contrave ER + Low-calorie Meal Box + Nutritional Intervention

Experimental

Drug: Contrave ER Combination Product: Low-calorie Meal Box Behavioral: Nutritional Intervention

干预措施: Contrave ER (Drug)

Contrave ER + Low-calorie Meal Box + Nutritional Intervention

Experimental

Drug: Contrave ER Combination Product: Low-calorie Meal Box Behavioral: Nutritional Intervention

干预措施: Low-calorie meal box (Combination Product)

Contrave ER + Conventional Nutritional Education

Active Comparator

Drug: Contrave ER Behavioral: Conventional Nutritional Education

干预措施: Contrave ER (Drug)

结局指标

主要结局

Remission

时间窗: From enrollment to the end of treatment at 12 weeks

The diabetes remission rate at Week 12 will be compared between the intervention and control groups relative to baseline. Remission of type 2 diabetes is defined, in accordance with the 2021 consensus report by American and European experts (Diabetes Care 2021;44:2438-44), as an HbA1c level of less than 6.5% at the end of the 12-week intervention, following discontinuation of all glucose-lowering medications at baseline.

次要结局

  • Body weight(Assessments will be performed at baseline and week 12. For participants who consent to the extension of the study period, additional assessments will be conducted at weeks 18 and 24.)

研究者

发起方
Yeouido St. Mary's Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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