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Completed

NCT Number: NCT01255020

Renal Protective Effects of Restricted Protein Dietary With α-keto Acid in CAPD Patients

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.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The 1st Affiliated Hospital, Sun Yet-sen University

Guangzhou, Guangdong, 510080, China

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients on peritoneal dialysis (PD) at least three month prior to study entry.
  • Subjects of either sex, more than 18 years old, the range of age is 18 to 70 year old.
  • Residual GFR ≥ 3 ml/min/1.73m2.
  • Without α-Keto Acid therapy in recent 4 weeks.
  • Subjects who agree to participate in the study and sign the informed consent.

Exclusion criteria

  • History of peritonitis or other infection within one month.
  • Patients with insufficient dialysis.
  • History of taking drug which may influence amino acid metabolism within one month(glucocorticoid, thyroxin, antithyroid drug, androgens,amino acids,et al).
  • Patients with diseases which contraindicate ketosteril.
  • Cannot control diet according to protocol.
  • Alcohol abuse or drug abuse.
  • Having malignant tumor.
  • History of psychiatric or neuropathic dysfunction.
  • 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)
  • Serum albumin < 30g/l.
  • Serum calcium > 2.8mmol/l.
  • Participation in another clinic trial within last three months

Treatment and study plan

α-Keto Acid with restricted protein diet

Drug

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

Other names: Test Group

Placebo plus restricted protein diet

Drug

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.

Other names: Control Group

Primary outcomes

  1. The longitudinal change in residual glomerular filtration rate (GFR)

    Time frame: Every 3 months up to 12 months

Secondary outcomes

  1. Peritoneal membrane transport characteristics

    Time frame: Every 3 months up to 12 months

  2. Cardiovascular events

    Time frame: Every 3 months up to 12 months

  3. Nutritional status

    Time frame: Every 3 months up to 12 months

  4. Hospitalization

    Time frame: Every 3 months up to 12 months

Sponsors and collaborators

Lead sponsor

Sun Yat-sen University

Other

Collaborators

  • Beijing Fresenius Kabi Pharmaceutical Co

Registry information

Official study title

Safety and Efficacy Evaluation of Restricted Protein Dietary Supplemented With α-keto Acid on Protecting Residual Renal Function in CAPD Patients--A Prospective, Double Blind Randomized, Parallel Control, Multi-center Clinical Trial

Important dates

Study start
2010
Primary completion
2013
Study completion
2013
First posted
Dec 7, 2010
Registry last updated
May 22, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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