跳至主要内容
临床试验/NCT03766334
NCT03766334撤回不适用

Efficacy and Safety of Highland Barley Diet on Glucose Variability in Patients With Type 1 Diabetes Mellitus

Huazhong University of Science and Technology1 个研究点 分布在 1 个国家开始时间: 2018年12月5日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Average blood glucose fluctuations at endpoint and baseline

研究概览

简要总结

Approximately 80 patients will be enrolled in the study from China and randomized in a 1:1 ratio to one of the 2 treatment arms:diabetes diet+highland barley diet; or diabetes diet.

Study treatment will continue for 12 weeks. The primary efficacy measure is the change in MAGE from continuous glucose monitoring system at 12 weeks. The study consists of 3 periods: a 1-week screening (period A), a 8-day run-in period (period B) and a 12-week treatment period (period C). Continuous glucose monitoring system will be used in baseline and endpoint.

详细描述

This is a prospective, randomized, open-label comparison of the effects and safety of barley meal plus diabetes diet on blood glucose fluctuations in patients with type 1 diabetes (T1DM) using multiple daily insulin injections (MDI). , parallel test. About 80 patients with T1DM were enrolled in the preliminary trial. During the lead-in period, no interventions were given to the patient's diet from day 1 to day 4, and diabetes diet education and guidance were given from day 5 to day 8, depending on the patient's blood glucose and diet. Personalization of habits, weights, and activities, etc., establish a diabetes diet. At the end of the lead-in period, patients were randomly divided into two treatment groups according to the ratio of 1:1: Observation group: Diabetes diet + barley diet. (The barley meal group diet was formulated according to the diabetes diet, but each meal was replaced with 20g barley nutrition powder and other calories instead of part of the diet. In the control group: Diabetes diet; dietary treatment after randomization will continue for 12 weeks. From the induction period to the treatment period 6 days, treatment period 10-12 weeks

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
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • type 1 diabetes patients with disease duration more than one year
  • HbA1c ≥7.0 % and < 11.0 %
  • Men and women (non-pregnant and using a medically approved birthcontrol method) aged ≥ 18 and ≤ 65 years
  • BMI ≥ 18 and ≤ 26 kg/m2

排除标准

  • Type 2 diabetes or other specific types of diabetes
  • Pregnancy, preparation for pregnancy, lactation and women of childbearing age incapable of effective contraception methods
  • Uncooperative subject because of various reasons
  • Abnormal liver function, glutamic-pyruvic transaminase (ALT) and glutamic-oxaloacetic transaminase (AST) > twice the upper limits of normal
  • Impairment of renal function, serum creatinine: ≥ 133mmol/L for female,≥ 135mmol/L for male
  • Serious chronic gastrointestinal diseases
  • Serious heart diseases, such as cardiac insufficiency (level III or more according to NYHA), acute coronary syndrome and old myocardial infraction
  • Blood pressure: Systolic blood pressure (SBP) ≥ 180mmHg and/or diastolic blood pressure (DBP) ≥ 110mmHg
  • White blood count (WBC) < 4.0×109/L or platelet count (PLT) < 90×109/L,or definite anemia (Hb:< 120g/L for male, < 110g/L for female), or other hematological diseases
  • Endocrine system diseases, such as hyperthyroidism and hypercortisolism
  • Experimental drug allergy or frequent hypoglycemia
  • Psychiatric disorders, drug or other substance abuse
  • Diabetic ketoacidosis and hyperosmolar nonketotic coma requiring insulin therapy
  • Stressful situations such as surgery, serious trauma and so on
  • Chronic hypoxic diseases such as pulmonary emphysema and pulmonary heart disease
  • Combined use of drugs effecting glucose metabolism such as glucocorticoid Tumor, especially bladder tumor and/or family history of bladder tumor and/or long-term hematuria

结局指标

主要结局

Average blood glucose fluctuations at endpoint and baseline

时间窗: from baseline to 12-week endpoint

Objective to investigate the effect of combination diabetes diet and highland barley diet on glucose variability in insufficient control patients with type 1 diabetes.

次要结局

  • Body mass index(endpoint)-Body mass index(baseline)(from baseline to 12-week endpoint)
  • Glycated hemoglobin(endpoint)-Glycated hemoglobin(baseline)(from baseline to 12-week endpoint)
  • beta-cell function at endpoint and baseline(from baseline to 12-week endpoint)
  • Waist circumference(endpoint)-Waist circumference(baseline)(from baseline to 12-week endpoint)
  • insulin dose(endpoint)-insulin dose(baseline)(from baseline to 12-week endpoint)
  • Quality of life assessment scale SF-36(endpoint)-Quality of life assessment scale SF-36(baseline)(from baseline to 12-week endpoint)

研究者

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

Xuefeng Yu

Chief of Department of Endocrinology

Huazhong University of Science and Technology

研究点 (1)

Loading locations...

相似试验

Efficacy and Safety of Highland Barley Diet on... | 临床试验