- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07587918
Sweet & Sour: Dietary Acid Load in Type 2 Diabetes and Kidney Disease Across Sex and Ethnic Groups (Sweet & Sour)
Sweet & Sour: Exploring Dietary Acid Load in Type 2 Diabetes & Kidney Disease Across Sex and Ethnicity
Chronic kidney disease (CKD) is a common condition and a major global cause of illness and mortality. The most common cause of kidney damage is diabetes, a condition that disrupts metabolism, leading to increased risk of damage to the kidneys and blood vessels. There is evidence suggesting that a diet with high acid load - consisting of acid-forming foods such as meat, cheese, and grain products - may contribute to this damage. People with such a diet often have poorer blood sugar control and more kidney damage. However, it is not yet well understood whether reducing dietary acid load can improve kidney function and diabetes management. Additionally, the role of ethnicity and sex in this process remains insufficiently explored.
The goal of this clinical trial is to understand how diet affects kidney function and blood sugar regulation in individuals with diabetes type 2 and chronic kidney disease, as well as to explore the role of sex and ethnicity in these effects. The main questions it aims to answer are:
Does a diet with lower acid load (e.g. less meat, cheese, and grain products) improve kidney function and blood sugar regulation in people with diabetes type 2 and chronic kidney disease?
Does the effect of diet on kidney function and blood sugar differ between ethnic groups, specifically between White-Dutch and South-Asian Surinamese descent people?
Participants will:
- be randomly assigned to follow either a high- or low-acid load diet for 8 weeks;
- Visit the study center four times (including screening)
- Complete food diaries three times per week and keep in regular contact with a dietitian;
- Collect 2x24-hour urine samples and morning feces at each visit ;
- Undergo blood sampling and an oral glucose tolerance test (OGTT).
- Spend a total of 8 hours at the study center (2 visits of 3 hours for OGTT and body composition tests, and 2 visits of 1 hour for additional assessments);
- Have up to 200 ml of blood collected during the study.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Ilias Attaye, Dr.
- Numéro de téléphone: +31 10 704 0704
- E-mail: i.attaye@erasmusmc.nl
Lieux d'étude
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Rotterdam, Pays-Bas
- Erasmus Medical Center
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Contact:
- Ilias Attaye, Dr.
- Numéro de téléphone: +31 10 704 0704
- E-mail: i.attaye@erasmusmc.nl
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Chercheur principal:
- Ilias Attaye, Dr.
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Sous-enquêteur:
- Dagmar Dekker, MSc
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Age >18 years
- Presence of T2D and CKD stage G1-3a with albuminuria (>10mg/mmol)
- BMI≥ 25kg/m2 - Use of metformin on a stable dose (i.e. no changes in the last three months)
- Adequate knowledge of the Dutch language to comprehend the provided study information
- If incretin therapy is used, then subject must have used that for a minimum of 6 months before starting with the trial
- Use of ACE inhibitors or angiotensin II receptor blokkers
- Of white European Dutch or South-Asian Surinamese descent
Exclusion Criteria:
- Use of insulin
- serum bicarbonate < 20 mmol/L
- Use of antibiotics 3 months before inclusion
- Vegetarian diet - Presence of inflammatory bowel disease or other chronic inflammatory disease
- Alcohol consumption of more than 14 units per week in women, or more than 21 units per week in men
- Active malignancy - bariatric or other weight loss surgery in the history
- patients diagnosed with eating disorders (such as bulimia nervosa, anorexia nervosa or binge-eating disorder)
- HbA1c >9% (75mmol/mol) at screening
- Unmotivated or not able to adhere to a specific diet
- The subject is already currently involved in a clinical trial
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: La prévention
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Aucune intervention: High Dietary Acid Load
This arm will follow their usual diet, which is between DAL> 50 or <120mEq H⁺/day (current western diets are generally all high DAL)
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Expérimental: Low Dietary Acid Load
This arm will follow a DAL lowering diet with the aim to reach <25mEq H⁺/day
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This arm will follow a DAL lowering diet with the aim to reach <25mEq H⁺/day
Autres noms:
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Percentage change in urinary albumin-to-creatinine ratio (UACR)
Délai: Change between baseline and 8 weeks
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Log-transformed urinary albumin-to-creatinine ratio (UACR), following an 8-week dietary intervention.
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Change between baseline and 8 weeks
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in estimated glomerular filtration rate (eGFR)
Délai: Change between baseline and 8 weeks
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eGFR calculated using serum creatinine and/or cystatin C
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Change between baseline and 8 weeks
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Change in serum bicarbonate
Délai: Change between baseline and 8 weeks
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Serum bicarbonate concentration measured in blood
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Change between baseline and 8 weeks
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Change in urinary citrate
Délai: Change between baseline and 8 weeks
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Urinary citrate excretion measured in 24-hour urine collections
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Change between baseline and 8 weeks
|
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Glucose response during Oral Glucose Tolerance Test
Délai: Change between baseline and 8 weeks
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Area under the curve (AUC) of plasma glucose during oral glucose tolerance test (OGTT)
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Change between baseline and 8 weeks
|
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Change in glucose variability (MAGE)
Délai: Change between baseline and 8 weeks
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Mean amplitude of glycemic excursions (MAGE) derived from continuous glucose monitoring (CGM) data.
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Change between baseline and 8 weeks
|
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Change in gut microbiota composition
Délai: Change between baseline and 8 weeks
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Gut microbiota composition assessed in morning fecal samples collected using stool collection kits analyzed by 16S rRNA gene sequencing.
|
Change between baseline and 8 weeks
|
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Change in serum metabolite profiles
Délai: Change between baseline and 8 weeks
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Serum metabolite profiles measured using untargeted metabolomics analysis.
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Change between baseline and 8 weeks
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Ilias Attaye, Dr., Erasmus Medical Center
Publications et liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Maladies urogénitales
- Maladies du système endocrinien
- Processus pathologiques
- Maladies urogénitales masculines
- Maladies rénales
- Maladies urologiques
- Maladies urogénitales féminines
- Maladies urogénitales féminines et complications de la grossesse
- Maladie chronique
- Attributs de la maladie
- Maladies métaboliques
- Troubles du métabolisme du glucose
- Diabète sucré
- Insuffisance rénale
- Conditions pathologiques, signes et symptômes
- Maladies nutritionnelles et métaboliques
- Diabète sucré, Type 2
- Insuffisance rénale chronique
Autres numéros d'identification d'étude
- NL-010928
Plan pour les données individuelles des participants (IPD)
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Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
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