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Completed

NCT Number: NCT01315314

Effect of Glucose Degradation Products (GDP) on Endothelial Dysfunction

The purpose of this study is to evaluate the effects of neutral pH and low glucose degradation product (GDP)-containing peritoneal dialysis fluid (PDF) on systemic inflammation and endothelial dysfunction markers in incident PD patients.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Division of Nephrology and Department of Internal Medicine, Kyungpook National University Hospital

Daegu, 700-721, South Korea

About this study

New peritoneal dialysis fluids (PDF) with neutral pH and low glucose degradation products (GDPs) are used in patients on peritoneal dialysis (PD). Low GDP fluids are reported to be more biocompatible than conventional PDF. Determination of biocompatibility has mainly focused on local peritoneal effects; recently, there has been interest in evaluating the systemic biocompatibility of these fluids.

In recent analyses of two retrospective cohorts of Korean PD patients, significant survival advantage was shown for patients treated with the biocompatible PDF compared to patients treated with conventional PDF. However, the mechanisms of survival advantage with low GPD PDF in these observational studies are difficult to assess. Additionally, it is not clear that new PDFs favorably impact risk markers of cardiovascular disease (CVD).

Epidemiologic studies identified an independent association between inflammation and risk of cardiovascular events and mortality; this association has been confirmed in patients with advanced chronic kidney diseases (CKD).Other evidence showed that clinically overt vascular events are preceded by endothelial dysfunction and increases in circulating markers of endothelial activation, including vascular cellular adhesion molecule (VCAM)-1 and intercellular adhesion molecule (ICAM)-1.Moreover, there is an association between inflammation and elevated levels of soluble VCAM-1 and ICAM-1 in patients with or at risk of atherosclerosis. Elevated levels of soluble adhesion molecules are found in ESRD patients, especially in patients with CVD and malnutrition.

The investigators hypothesized that conventional PDF as well as uremia itself lead to local peritoneal changes such as peritoneal neoangiogenesis and fibrosis, effects related to ultrafiltration failure and subsequently volume overload. In addition, direct effect of GDPs and/or increased systemic levels of AGEs activate endothelial cells and increase levels of vascular adhesion molecules and inflammation. Both local and systemic effects of PDF are possibly associated with increased cardiovascular risks and mortality in PD patients.

This study aims to examine the effects of neutral pH and low GDP-containing PDF on systemic inflammation and endothelial dysfunction in incident PD patients in a randomized, controlled study.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Male and female patients aged over 18 years and less than 75 years
  • Within 90 days of initiation of first renal replacement treatment for ESRD
  • Selected for maintenance management by CAPD
  • Having provided informed consent
  • Physically and mentally capable of performing the therapy

Exclusion criteria

  • Patients were excluded if deemed to have less than 80% likelihood of survival for at least 1 year
  • episodes of peritonitis within prior 30 days
  • any malignancy other than treated skin carcinoma
  • uncontrolled congestive heart failure
  • recent (within 60 days) myocardial infarction or cerebrovascular accident
  • active systemic vasculitic disease including systemic lupus erythematosus, polyarteritis nodosa, ANCA-nephritis, active rheumatoid disease, or active venous thrombotic-embolic disease
  • any acute infection at the time of enrollment
  • active or actively treated tuberculosis
  • recent (within 30 days) systemic bacterial infection.

Treatment and study plan

Balance, Fresenius Medical Care, Germany

Drug

low glucose degradation product (GDP)-containing peritoneal dialysis fluid (PDF)

Other names: Balance, Fresenius Medical Care

Primary outcomes

  1. Inflammation-endothelial-dysfunction index (IEDI)

    Time frame: Baseline and 12 months

    Inflammation-endothelial-dysfunction index (IEDI) is a composite score derived from measurement of serum levels of CRP (high sensitivity assay), soluble VCAM-1 and soluble ICAM-1. Changes between the groups will be tested by analysis of covariance (ANCOVA) with baseline values as covariates. Serial data will also be analyzed using a linear mixed model.

Secondary outcomes

  1. Individual component markers of IEDI

    Time frame: Baseline and 12 months

    individual component markers of the IEDI including sICAM-1, sVCAM-1, and hs-CRP

  2. RRF

    Time frame: Baseline and 12 months

    residual renal function (RRF) as average of urea and creatinine clearances by 24 hour urine collection

  3. peritoneal clearance

    Time frame: Baseline and 12 months

    peritoneal clearance as weekly Kt/V urea and creatinine clearance

  4. peritoneal ultrafiltration

    Time frame: Baseline and 12 months

    peritoneal ultrafiltration volume

  5. peritoneal transport status

    Time frame: Baseline and 12 months

    dialysate-to-plasma ratio of creatinine at 4 hours of peritoneal equilibration test

  6. serum albumin

    Time frame: Baseline and 12 months

  7. LBM

    Time frame: Baseline and 12 months

    lean body mass (LBM) estimated from creatinine kinetics

  8. nPNA

    Time frame: Baseline and 12 months

    normalized protein equivalent of nitrogen appearance (nPNA)

  9. SGA

    Time frame: Baseline and 12 months

    subjective global assessment (SGA) with a four item and seven-point scale

  10. Blood pressure

    Time frame: Baseline and 12 months

    systolic and diastolic blood pressure

  11. use of antihypertensive medications

    Time frame: Baseline and 12 months

    number of antihypertensive medications

  12. peritonitis rates

    Time frame: 12 months

    peritonitis rates

  13. technique survival

    Time frame: 12months

    technique survival by Kaplan-Meier survival analysis with Log-Rank test.

  14. patient survival

    Time frame: 12 months

    patient survival by Kaplan-Meier survival analysis with Log-Rank test.

Sponsors and collaborators

Lead sponsor

Kyungpook National University Hospital

Other

Collaborators

  • Fresenius Medical Care Korea
  • Ministry of Health & Welfare, Korea

Registry information

Official study title

Effects of Neutral pH and Low Glucose Degradation Product-containing Peritoneal Dialysis Fluid on Systemic Markers of Inflammation and Endothelial Dysfunction: a Randomized, Controlled 1-year Follow-up Study

Important dates

Study start
2005
Primary completion
2008
Study completion
2008
First posted
Mar 15, 2011
Registry last updated
Mar 17, 2011

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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