NCT00999453

Brief Summary

Cardiovascular disease (CVD) is the leading cause of morbidity and mortality in dialysis patients. Although significant improvements have been made in the management of CVD in the general population, it is not known whether these interventions would result in similar benefits in end stage renal disease patients. Clinical studies conducted in the general population and in patients with established cardiovascular disease have found a strong independent association between lipid lowering, primarily LDL-cholesterol, and the risk of all-cause and cardiovascular mortality. Therefore the National Cholesterol Education Panel (NCEP) has provided guidelines to lower LDL cholesterol levels to a goal of ≤100 mg/dl in patients with major risk factors of coronary heart disease. Moreover, the recent Adult Treatment Panel III (ATP III) guidelines provide an option to lower LDL cholesterol levels to a goal of \<70 mg/dl in patients with very high risks for coronary heart disease. The National Kidney Foundation K/DOQI guideline regards dialysis patients as having high risks for coronary heart disease and consequently recommends the LDL cholesterol level to be maintained under 100 mg/dl. This recommendation is in parallel to the NCEP ATP III guideline which has been proposed for the general population. However, data regarding cholesterol levels in dialysis patients have been conflicting, with some observational studies demonstrating and some not demonstrating a clear, relationship between LDL and cardiovascular end-points. In addition few randomized studies have been conducted in CKD patients. An observational retrospective analysis of patients receiving hemodialysis, the U.S. Renal Data System Morbidity and Mortality Study, showed that the risk for cardiovascular mortality was decreased by 36 percent among patients receiving statins, compared to those who did not. Whereas, a most recent large prospective study in diabetic hemodialysis patients failed to demonstrate a significant reduction in cardiovascular endpoints with statin therapy. Moreover, although HD and PD patients both develop chronic hypervolemia and inflammation as common findings, the relationship between risk factors and outcome may differ between these two treatment methods. The likely role of glucose from the dialysate in causing dyslipidemia in PD patients inherits a different strength of association between cholesterol level and outcome in HD and PD patients. Therefore, this study aims to examine the clinical outcomes of treating chronic peritoneal dialysis patients with dyslipidemia to lower cholesterol levels, randomly assigning patients to either aggressive targets of LDL cholesterol of 70 mg/dl or current standard targets of LDLD cholesterol of 100 mg/dl.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
43

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2009

Longer than P75 for not_applicable

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2009

Completed
17 days until next milestone

First Submitted

Initial submission to the registry

October 18, 2009

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 21, 2009

Completed
6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2015

Completed
Last Updated

March 17, 2017

Status Verified

October 1, 2009

Enrollment Period

6.1 years

First QC Date

October 18, 2009

Last Update Submit

March 15, 2017

Conditions

Keywords

LDL-cholesterolPrevalent peritoneal dialysis patients with hypercholesterolemia

Outcome Measures

Primary Outcomes (1)

  • Cardiovascular complication including acute coronary syndrome, cerebrovascular infarction and cardiovascular death

    5 years (after detecting Cardiovascular complication)

Study Arms (2)

LDL-cholesterol 70 mg/dL or lower

EXPERIMENTAL

'Experimental arm' is defined as patients treated to lower the level of low-density lipoprotein to 70 mg/dl or lower. 'Control arm' is defined as patients treated to lower low-density lipoprotein to a level of 100 mg/dl or lower.

Other: LDL-cholesterol

LDL-cholesterol 100 mg/dL or lower

ACTIVE COMPARATOR

'Experimental arm' is defined as patients treated to lower the level of low-density lipoprotein to 70 mg/dl or lower. 'Control arm' is defined as patients treated to lower low-density lipoprotein to a level of 100 mg/dl or lower.

Other: LDL-cholesterol

Interventions

This is a 2-arm, open label, multi-center, randomized trial comparing aggressive to standard treatment of LDL-cholesterol. After screening, randomization, participants will be seen every 3 months during the follow-up period. An LDL-cholesterol 100 mg/dL is the goal for the standard group and the target for the aggressive group is 70 mg/dL. A lipid lowering algorithm has been developed based on the NCEP-ATP III recommendation which is used as a general guideline, allowing alterations based on the individual participants needs.

LDL-cholesterol 100 mg/dL or lowerLDL-cholesterol 70 mg/dL or lower

Eligibility Criteria

Age20 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • End-stage renal disease patients treated with peritoneal dialysis for 3 or more months
  • LDL cholesterol 100 mg/dl or higher within 3 months and total cholesterol level 220 mg/dl or higher

You may not qualify if:

  • Hypersensitivity to statin, ezetimibe, fenofibrate
  • Acute MI, angina, cerebrovascular accident, vascular intervention within the last 6 months
  • Chronic obstructive pulmonary disease
  • alanine transaminase \> 3 times the upper normal limit
  • creatine kinase \> 3 times the upper normal limit
  • Patients suffering form non-cardiac diseases with estimated survival less than 2 years
  • Inevitable of cyclosporin, warfarin use
  • Currently pregnant or breast feeding
  • Any condition that might limit long-term compliance (e.g., psychiatric disorders)
  • Participation in another clinical trial within 30 days prior to enrollment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Unknown Facility

Kyungpook National University Hospital, Daegu, South Korea

Location

Severance Hospital

Seoul, South Korea

Location

MeSH Terms

Conditions

Hypercholesterolemia

Interventions

Cholesterol, LDL

Condition Hierarchy (Ancestors)

HyperlipidemiasDyslipidemiasLipid Metabolism DisordersMetabolic DiseasesNutritional and Metabolic Diseases

Intervention Hierarchy (Ancestors)

CholesterolSterolsCholestanesSteroidsFused-Ring CompoundsPolycyclic CompoundsLipoproteins, LDLLipoproteinsLipidsMembrane LipidsProteinsAmino Acids, Peptides, and Proteins

Study Officials

  • Shin-Wook Kang, M.D., PhD.

    professor of division of Nephrology, Severance Hospital, Korea

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

October 18, 2009

First Posted

October 21, 2009

Study Start

October 1, 2009

Primary Completion

November 1, 2015

Study Completion

November 1, 2015

Last Updated

March 17, 2017

Record last verified: 2009-10

Locations