Effects of Exogenous Ketosis on Proteinuria and Renal Function
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Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Ketone Diol, R-1,3-butanediol (Ketone-IQ), Placebo drink.
- Кому может быть актуально
- Состояния в реестре: Renal Insufficiency, Chronic, Polycystic Kidney Diseases, Proteinuria, Ketosis. Базовые параметры: от 18 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Дания
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Effects of Exogenous Ketosis on Proteinuria and Renal Function in Patients with Chronic Kidney Disease and Patients with Polycystic Kidney Disease
Обзор
A randomized, placebo-controlled, double-blinded crossover study will be conducted. Fourteen patients with polycystic kidney disease (PKD) and 29 patients with proteinuric kidney disease will receive ketone bodies (Ketone-IQ) and placebo in a randomized order. Each treatment period is four weeks. There will be a wash-out period of two weeks in between treatment periods. Effect variables will be measured in the last day of each treatment period.
Подробное описание
Background: Until recently, the only treatment shown to slow progression of chronic kidney disease (CKD) has been angiotensin converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs).
The use of sodium glucose transporter 2 (SGLT2)-inhibitors, which work by blocking the activity of sodium-glucose-cotransporter 2 channels in the proximal kidney tubule, has completely transformed the treatment of proteinuric kidney disease, with a 28% decrease in the risk for cardiorenal outcomes. Despite these new treatment options, a significant proportion of patients still succumb to kidney failure, require hospitalization for heart failure and die prematurely. Thus, additional preventive measures are essential.
Renewed interest in the physiological role of ketone bodies (KB) has emerged. It has become increasingly clear that ketosis has several beneficial effects including anti-epileptic effects, improved exercise capacity, lipid profile, cardiac function and cognition.
However, only few clinical studies have studied renal effects of exogenous ketosis, and to our knowledge there are no clinical studies examining the effects long term effects of renal ketosis in patients with CKD.
Hypothesis: Ketosis decreases urine albumin to creatinine ratio (ACR) and glomerular filtration rate (GFR) in patients with CKD/PKD.
Methods: A randomized, placebo-controlled, double-blinded crossover study will be conducted. Twenty-nine patients with proteinuric kidney disease (study a) and 14 patients with PKD (study b) will receive ketone bodies (Ketone-IQ) and placebo in a randomized order. Each treatment period is four weeks. There will be a wash-out period of two weeks in between treatment periods. Effect variables will be measured in the last day of each treatment period.
Perspectives: The study has the potential to provide information regarding the therapeutic potential of ketone bodies in patients with CKD/PKD.
Вмешательства
- Пищевая добавка Ketone Diol, R-1,3-butanediol (Ketone-IQ)
Effect variables will be measured on the last day of treatment with Ketone-IQ - Другое Placebo drink
Effect variables will be measured on the last day of treatment with Placebo
Первичные конечные точки
- Proteinuria [Срок оценки: Measured on 24 hour urine collection on the last day in each treatment period (each treatment period is 4 weeks)]
- GFR [Срок оценки: Measured on the last day in each treatment period (each treatment period is 4 weeks)]
Вторичные конечные точки (9)
- Aldosterone [Срок оценки: Measured on the last day in each treatment period (each treatment period is 4 weeks)]
- P-Beta-hydroxybutyrate [Срок оценки: Measured on the last day in each treatment period (each treatment period is 4 weeks)]
- Excretion rate of renal tubular transport proteins [Срок оценки: Measured on the last day in each treatment period (each treatment period is 4 weeks)]
- 24-hour Ambulatory Blood Pressure [Срок оценки: Measured using a Mobil-o-graph on the last day in each treatment period (each treatment period is 4 weeks)]
- Sodium and potassium excretion [Срок оценки: Measured on 24 hour urine collection on the last day in each treatment period (each treatment period is 4 weeks)]
- Peripherial Vascular Resistance [Срок оценки: Measured using a Mobil-o-graph on the last day in each treatment period (each treatment period is 4 weeks)]
- Heart rate [Срок оценки: Measured using a Mobil-o-graph on the last day in each treatment period (each treatment period is 4 weeks)]
- Pulse Wave Velocity [Срок оценки: Measured using a Mobil-o-graph on the last day in each treatment period (each treatment period is 4 weeks)]
- Renin [Срок оценки: Measured on the last day in each treatment period (each treatment period is 4 weeks)]
Критерии участия
Критерии включения
Study A (patients with CKD):
- ACR > 200 mg/g <3000 mg/g
- eGFR >30 ml/min/1,73m2
- Treatment with Renin-Angiotension System (RAS) blockers and SGLT-2 inhibitors for a minimum of 4 weeks prior to inclusion
- Safe contraception if women in childbearing age
Study B (patients with PKD):
- Prior diagnose with PKD
- eGFR >30 ml/min/1,73m2
- Treatment with Renin-Angiotension System (RAS) blockers for a minimum of 4 weeks prior to inclusion
- Safe contraception if women in childbearing age
Exclusion Criteria (Study A+B)
- Diabetes Mellitus type 1
- Heart Failure
- Liver Disease
- Kidney transplant
- Malignant diseases (except skin cancer)
- Recent acute myocardial infarction (AMI), apoplexia/transient ischemic attack (TIA) (within 3 months of inclusion)
- Pregnancy or breast feeding
- Alcohol or drug abuse
- Periodic fasting within four weeks of inclusion
- Routinely intake of ketogenic diet within four weeks of inclusion
- Treatment with nitrate
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Перекрёстный дизайн
- Маскирование
- Четверное слепое
- Основная цель
- Профилактика
Центры проведения
Дания · 1 центр
- University Clinic in Nephrology and Hypertension, Gødstrup Region Hospital — Herning
Идентификаторы
NCT: NCT06867471 · TZL-2-2024