Pentraxin-3 in Chronic Renal Failure
- Conditions
- Chronic Kidney DiseaseInflammation
- Registration Number
- NCT01397773
- Lead Sponsor
- Haseki Training and Research Hospital
- Brief Summary
The aim of the study is to measure Pentraxin-3 levels in patients on hemodialysis, peritoneal dialysis and those in the pre-dialysis period; and to compare these groups with the control group; so as to investigate the eligibility of it as a reliable marker of inflammation; relationship with other inflammatory markers and carotis intima media thickness.
- Detailed Description
The investigators planned to involve four group of patients: Hemodialysis, peritoneal dialysis, pre-dialysis and the control group; with about 25 patients planned to be involved in each group. The laboratory parameters to be measured are Pentraxin-3, C-reactive protein (CRP), high sensitive CRP, fibrinogen and interleukin-6. Concomitantly, carotis intima media thickness will be measured in the radiology clinic. Statistical analysis will be carried on by Statistical Package for Social Sciences (SPSS) for Windows 13.0. The variables acting on the inflammatory parameters and the correlation between them and carotis intima media thickness will be studied.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 85
- To give informed consent
- Hemodialysis or peritoneal dialysis for more than 3 months
- Creatinin clearance less than 30 ml/min for the pre-dialysis group
- Not to give informed concent
- Active infection within the last 3 months
- Known chronic inflammatory disease
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pentraxin-3 level Five months Pentraxin-3 level will be compared with other inflammatory markers.
- Secondary Outcome Measures
Name Time Method Carotis intima media thickness Five months Correlation of Pentraxin-3 and carotis intima media thickness
Trial Locations
- Locations (1)
Haseki Training and Research Hospital
🇹🇷Istanbul, Turkey