Renal Function Disorder
Conditions
Keywords
α-Keto Acid, Restricted Protein Diet, Residual Renal Function
Brief summary
The prospective, double blind randomized, parallel control, and multi-center clinical trial will evaluate the safety and efficacy of α-keto acid with restricted protein diet on protecting residual renal function in continuous ambulatory peritoneal dialysis (CAPD) patients.
Detailed description
Residual renal function (RRF) is associated with cardiovascular complication, nutritional status, incidence of peritonitis, and quality of life in peritoneal dialysis (PD) patients. Therefore, RRF is an important determinant of mortality and morbidity in PD patients. Previous studies have suggested that dietary protein restriction supplemented with α-keto acids may slow the loss of RRF in chronic kidney disease patients. However, these trials are small sample and short-time research. In PD patients, there is very few reports to indicate the effect of α-keto acid with restricted protein diet on RRF. The aim of this study is to evaluate the safety and efficacy of α-keto acid with restricted protein diet on protecting residual renal function in continuous ambulatory peritoneal dialysis (CAPD) patients.This is a prospective, double blind randomized, parallel control, and multi-center clinical study. 160 patients who meet Inclusion/Exclusion criteria will be randomized into α-Keto Acid group or control group at the ratio of 1:1. The α-Keto Acid group will use compound α-Keto Acid plus restricted protein diet, while control group will use placebo plus restricted protein diet.The α-Keto Acid dosage is 100mg/kg/d daily. The restricted protein dosage is 1g/kg/d. The safety and efficacy of α-Keto Acid with restricted protein diet on RRF will be evaluated after 1 year treatment.
Interventions
α-Keto Acid: The daily dose of compound α-Keto Acid is 100mg/kg/d. The total daily dose will be divided into three times a day. Restricted Protein Diet: Diet contain protein 1.0g/kg/d
placebo: The daily dose of placebo is 100mg/kg/d. The total daily dose will be divided into three times a day. Diet contain protein 1.0 g/kg/d.
Sponsors
Study design
Eligibility
Inclusion criteria
1. Patients on peritoneal dialysis (PD) at least three month prior to study entry. 2. Subjects of either sex, more than 18 years old, the range of age is 18 to 70 year old. 3. Residual GFR ≥ 3 ml/min/1.73m2. 4. Without α-Keto Acid therapy in recent 4 weeks. 5. Subjects who agree to participate in the study and sign the informed consent.
Exclusion criteria
1. History of peritonitis or other infection within one month. 2. Patients with insufficient dialysis. 3. History of taking drug which may influence amino acid metabolism within one month(glucocorticoid, thyroxin, antithyroid drug, androgens,amino acids,et al). 4. Patients with diseases which contraindicate ketosteril. 5. Cannot control diet according to protocol. 6. Alcohol abuse or drug abuse. 7. Having malignant tumor. 8. History of psychiatric or neuropathic dysfunction. 9. Cardiac failure, with New York Heart Association (NYHA) grade III-IV or history of severe heart and cerebrovascular disease in recent one month(acute stroke, acute heart failure, Lability angina) 10. Serum albumin \< 30g/l. 11. Serum calcium \> 2.8mmol/l. 12. Participation in another clinic trial within last three months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The longitudinal change in residual glomerular filtration rate (GFR) | Every 3 months up to 12 months |
Secondary
| Measure | Time frame |
|---|---|
| Peritoneal membrane transport characteristics | Every 3 months up to 12 months |
| Cardiovascular events | Every 3 months up to 12 months |
| Nutritional status | Every 3 months up to 12 months |
| Hospitalization | Every 3 months up to 12 months |
Countries
China