跳至主要内容
临床试验/NCT07185555
NCT07185555招募中不适用

Applying Very Low Calorie Ketogenic Diet to the Treatment of Obesity in People With Type 1 Diabetes on Intensive Insulin Therapy Using Automated Insulin Delivery System

Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2025年1月16日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
14
试验地点
2
主要终点
Change in body weight from baseline to end of 4-week Very Low-Energy Ketogenic Therapy

研究概览

简要总结

Overweight and obesity are frequent in adults with type 1 diabetes (T1D), with prevalence exceeding 50% in recent studies. Excess weight in T1D is associated with higher cardiometabolic risk and therapeutic challenges, while effective and safe weight management strategies are still limited.

This single-center, single-arm feasibility study will evaluate the efficacy and safety of a Very Low-Energy Ketogenic Therapy (VLEKT; 600-800 kcal/day) in adults with T1D and obesity treated with Advanced Hybrid Closed Loop (AHCL) insulin delivery systems. Participants will follow a structured 4-week program with commercial very-low-carbohydrate, high-protein meal replacements, under close medical supervision.

The primary endpoint is change in body weight at 4 weeks. Secondary outcomes include body composition, muscle strength, glucose metrics, insulin requirements, biochemical parameters, and patient-reported outcomes. Safety will be assessed through hypoglycemia incidence, ketone monitoring, and occurrence of diabetic ketoacidosis (DKA).

The study will enroll 14 participants. It is expected that VLEKT will achieve ~5% weight loss within one month while maintaining glycemic safety under AHCL technology.

详细描述

Excess weight in type 1 diabetes (T1D) is increasingly recognized as a critical clinical problem. Factors contributing to weight gain include intensive insulin therapy, compensatory intake of high-energy foods to prevent hypoglycemia, reduced physical activity due to fear of hypoglycemia, and pathophysiological mechanisms such as adipose tissue dysfunction and insulin resistance. Current therapeutic options for weight management in T1D are limited compared with type 2 diabetes, and novel approaches are urgently needed.

Ketogenic and very low-carbohydrate diets are effective in obesity and type 2 diabetes but have traditionally been discouraged in T1D because of risks of hypoglycemia, dyslipidemia, poor adherence, and diabetic ketoacidosis (DKA). The introduction of Advanced Hybrid Closed Loop (AHCL) systems, which combine continuous glucose monitoring with automated insulin delivery, provides a safer framework to test structured dietary interventions that were previously considered unsuitable in this population.

This feasibility study investigates a Very Low-Energy Ketogenic Therapy (VLEKT) for 4 weeks in adults with T1D and obesity using AHCL technology. The intervention will consist of commercially available meal replacements (600-800 kcal/day, <30 g/day carbohydrates, adequate protein supply) with strict monitoring of capillary ketones and insulin adjustments.

Baseline assessments include anthropometry, bioimpedance-derived body composition, handgrip strength, biochemical testing, continuous glucose monitoring metrics, and validated questionnaires (SF-12, IPAQ, PSQI, FH-15). Participants will attend weekly visits for clinical review, adherence reinforcement, safety checks, and repeat assessments. At study completion, a gradual reintroduction of conventional meals will be initiated.

The primary endpoint is absolute weight change after 4 weeks. Secondary endpoints include proportion achieving ≥5% weight loss, changes in body composition and muscle strength, glucose control (TIR, TAR, TBR, CV, GMI, GRI, TITR), insulin requirements, lipid and liver function markers, and patient-reported outcomes. Safety evaluation will focus on hypoglycemia incidence and DKA events.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years
  • Diagnosis of type 1 diabetes or autoimmune diabetes for ≥ 12 months
  • BMI ≥ 30 kg/m²
  • HbA1c < 9%
  • Knowledge and use of carbohydrate counting
  • Use of an Advanced Hybrid Closed Loop (AHCL) system for ≥ 3 months and willingness to maintain it during the study
  • At least 1 diabetology follow-up visit in the last 12 months (including telemedicine)
  • Willingness to purchase meal replacements for the entire study duration

排除标准

  • Ketoacidosis, severe hypoglycemia with seizures/coma, or severe hyperglycemia requiring hospitalization in the last 6 months
  • Febrile illness within the last 2 weeks
  • Dietary restrictions or intolerances incompatible with study food supplies
  • Celiac disease, gastroparesis, food allergies
  • Intense physical exercise >2 hours on >3 days per week
  • History or risk of eating disorder, or other psychiatric disorders
  • Recreational drug use or excessive alcohol consumption
  • Chronic kidney disease (eGFR <60 ml/min)
  • Liver failure
  • Heart failure (NYHA III-IV), unstable angina, cardiac arrhythmia, myocardial infarction, or stroke within the last 12 months
  • Respiratory failure
  • Severe or active infections
  • Planned elective surgery
  • Rare metabolic diseases (porphyria, CPT2 deficiency, mitochondrial fatty acid oxidation defect, pyruvate carboxylase defect)
  • Pregnancy (current or actively trying to conceive)
  • Breastfeeding
  • Current glucocorticoid therapy (except stable low-dose, inhaled, or replacement for adrenal insufficiency)
  • Other serious medical conditions that might interfere with participation or study completion in the investigator's judgment
  • Participant judged unable or unwilling to complete the study

结局指标

主要结局

Change in body weight from baseline to end of 4-week Very Low-Energy Ketogenic Therapy

时间窗: Baseline and Week 4

Body weight will be measured in kilograms using a calibrated scale at baseline and after completion of the 4-week intervention. The primary outcome is the absolute change in weight from baseline. Participants will be assessed under standardized conditions (light clothing, no shoes, fasting state where possible).

次要结局

未报告次要终点

研究者

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

Francesco Giorgino

Professor of Endocrinology, Director of Department of Precision and Regenerative Medicine and Ionian Area, Chief of Division of Endocrinology - University Hospital Policlinico Consorziale

Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari

研究点 (2)

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