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临床试验/NCT06618859
NCT06618859招募中不适用

Time-restricted Eating in Patients With Moderate Chronic Kidney Disease and Albuminuria: A Pilot Randomized, Open-label, Double-arm Trial (TRECK)

de Seigneux Sophie2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年12月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
50
试验地点
2
主要终点
Change in urine albumin/creatinine ratio (UACR)

研究概览

简要总结

Chronic kidney disease (CKD) affects approximately 12 to 15% of adults worldwide, with an increasing incidence expected. Major causes include diabetic nephropathy, hypertension, and various glomerulonephritis. Proteinuria is a key factor in identifying and assessing the risk of CKD progression.

The precise pathophysiology of CKD is not fully understood, but recent research highlights metabolic alterations, particularly in lipid and glucose metabolism. CKD progression is influenced by diet, as evidenced by recent studies. Interventions such as the ketogenic diet and time-restricted feeding show promising results in improving metabolism and may have beneficial effects on CKD.

Our study aims to evaluate the impact of time-restricted eating (TRE) on proteinuria, the decline in glomerular filtration rate, and weight loss in patients with moderate CKD with albuminuria (KDIGO stage 2-3). This will allow us to better understand the efficacy of this dietary approach tailored to the individual habits of participants.

The primary outcome measure will be albuminuria before and after the 12-week intervention. Secondary outcome measures will include the impact of fasting on blood pressure as assessed by 24-hour ambulatory monitoring, body composition evaluated by DXA and BIA, continuous glucose monitoring, and blood hormone profiles. Additionally, the feasibility and safety of TRE in this population will be assessed.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Clinical criteria
  • Adult men and women
  • Chronic Kidney Disease with KDIGO stage G2 and G3 defined by a Glomerular Filtration Rate between 30 and 90 mL/min/1.73m2
  • Albuminuria stage A2 or A3, but without nephrotic-range proteinuria: 3 to 200 mg/mmol
  • Body mass index 18-40 kg/m2
  • Eating window of 12 hours (self-reported and measured during the run-in phase)
  • Study-related criteria
  • Able to give informed consent and follow the study procedures for the entire duration
  • Confident use of a smartphone compatible with the MyFoodRepo app (iOS, Android) and able to take regular pictures of food/drinks

排除标准

  • Clinical criteria
  • Pregnant and breastfeeding women, plans for maternity during the study
  • Eating disorder(s)
  • Other diets: low-carb, ketogenic diet, hypocaloric diets (eviction for food intolerances, vegan/vegetarian diet are not excluded)
  • Uncontrolled blood pressure (> 160/100 mmHg)
  • Diabetes with hypoglycemic drug(s) will be excluded, however those with impaired glucose tolerance (prediabetes, as defined by the American Diabetes Association) or diabetes with no risk of hypoglycemia (i.e. treated with non-hypoglycemic drugs or without medication) will be included
  • Oral corticosteroids
  • Uncontrolled diabetes HbA1c > 8.5%
  • Active cancer and/or oncologic treatment over the previous 12 months
  • Major mental illness
  • Consumption of > 7 standard units of alcohol per week for women and > 14 standard units of alcohol per week for men
  • Shift work, such as evening shifts or night shifts planned during the study
  • Travel/trip to a different time zone (≥ 2-hour time difference) planned during the study
  • Study-related criteria and other interventions
  • Recent treatment modification in the last 3 months, including but not limited to ACE blockers, SLGT2i, finerenone
  • Patients with recent glomerulonephritis diagnosis on more than 2 immunosuppressive drugs
  • Patients with kidney transplant in the last past year
  • Enrolled in another interventional clinical trial (medication, medical device) over the previous 1 month and planned during the study

研究组 & 干预措施

Active control

Active Comparator

干预措施: Active control (Behavioral)

Time-restricted eating

Experimental

干预措施: Time-restricted eating (Behavioral)

结局指标

主要结局

Change in urine albumin/creatinine ratio (UACR)

时间窗: From randomization to close-out visit (12 weeks)

Measured by 24h urine collection

次要结局

  • Change in creatinine- and cystatin-estimated glomerular filtration rate (eGFR)(From randomization to close-out visit (12 weeks))
  • Change in blood pressure(From randomization to close-out visit (12 weeks))
  • Change in systolic and diastolic blood pressure(From randomization to close-out visit (12 weeks))
  • Change in body fat mass and regional distribution(From randomization to close-out visit (12 weeks))
  • Change in body fat mass(From randomization to close-out visit (12 weeks))
  • Change in fasting glucose(From randomization to close-out visit (12 weeks))
  • Change in glucose excursion(From randomization to close-out visit (12 weeks))
  • Change in physical activity(From randomization to close-out visit (12 weeks))
  • Change in sleep/wake cycles(From randomization to close-out visit (12 weeks))
  • Change in sleep quality(From randomization to close-out visit (12 weeks))
  • Change in eating duration(From randomization to close-out visit (12 weeks))
  • Change in weight(From randomization to close-out visit (12 weeks))
  • Change in lipid profile (concentration of total cholesterol, LDL cholesterol, HDL cholesterol, triglycerides)(From randomization to close-out visit (12 weeks))
  • Change in blood hormone profile(From randomization to close-out visit (12 weeks))
  • Incidence of adverse events in response to the randomized intervention(From randomization to close-out visit (12 weeks))

研究者

发起方
de Seigneux Sophie
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

de Seigneux Sophie

Principal Investigator

University Hospital, Geneva

研究点 (2)

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