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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02072837
Other study ID # E.S.931/5-12-2006
Secondary ID
Status Completed
Phase N/A
First received February 25, 2014
Last updated February 27, 2014
Start date January 2012
Est. completion date January 2014

Study information

Verified date February 2014
Source National and Kapodistrian University of Athens
Contact n/a
Is FDA regulated No
Health authority Greece: Ethics Committee
Study type Observational

Clinical Trial Summary

In this study, we studied lipoprotein abnormalities-related variables as risk factors for the development of cardiovascular disease in patients on renal replacement therapies.We studied 96 dialyzed patients, 62 males and 34 females, on mean age 62.1 years old and 24 healthy controls.We concluded that metabolic acidosis activating the inflammation and lipoprotein oxidation influences the dyslipidemia and cardiovascular morbidity of patients on renal replacement therapies.Dialysis adequacy was positively associated to cardioprotective HDL.Peritoneal dialysis holds a better acidosis level and lower oxidized lipids than hemodialysis modalities.


Description:

Blood samples were obtained by venipuncture in the peritoneal dialyzed patients and control group in a twelve hours fasting state.In hemodialyzed patients blood was drawn just before the start of the mean weekly dialysis session also in a twelve hours fasting state from the vascular access.

All samples were received once at baseline time ( in the start of the study ). Peripheral systolic and diastolic blood pressures were calculated as an average of 10 measurements during a renal replacement treatment month in the starting time of the study.

Also, electrocardiographic examination, echocardiography and the calculation of ankle-brachial blood pressure index became once in the start of the study.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date January 2014
Est. primary completion date January 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 24 Years to 87 Years
Eligibility Inclusion Criteria:

- permanent renal replacement therapy more than 6 months and

- accurate dry body weight

Exclusion Criteria:

- acute illness,

- significant infection,

- malignancy,

- Kt/V for urea <1.2.

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
National and Kapodistrian University of Athens

Outcome

Type Measure Description Time frame Safety issue
Primary Associations between dyslipidemia with cardiovascular disease on patients on renal replacement therapy February 2014 No
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