Mineral Bone Disorder in Dialysis

Çanakkale Onsekiz Mart University167 enrolled

Overview

This study was conducted with 167 dialysis patients at Erciyes University Faculty of Medicine, Department of Internal Medicine, Department of Nephrology, and Dialysis Unit, with the approval of the Ethics Committee of Erciyes University Medical Faculty (date: 25.09.2019, no: 2019/673). Patients aged ≥18 years, undergoing dialysis treatment, and having available data on serum calcium, phosphorus, parathormone, albumin, hemoglobin, blood urea nitrogen (BUN), creatinine, and dialysate calcium levels within the last six months were included in the study.

Study Type

OBSERVATIONAL

Enrollment

167

Conditions

Chronic Kidney Failure Chronic Kidney Disease-Mineral and Bone Disorder Dialysis Hemodialysis

Interventions

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Age ≥ 18 years, * Diagnosed with chronic kidney disease (CKD) and undergoing dialysis treatment (hemodialysis or peritoneal dialysis) * Availability of laboratory results within the last 6 months: serum calcium, phosphorus, parathormone, albumin, hemoglobin, blood urea nitrogen (BUN), creatinine, and dialysate calcium * Patient consent to participate Exclusion Criteria: * Age \< 18 years * Patients not on dialysis treatment * Missing or incomplete laboratory data * History of malignancy, acute infection, or other systemic diseases interfering with mineral and bone metabolism * Patients who did not provide consent or could not complete the questionnaire

Locations (1)

Erciyes University Hospital, Faculty of Medicine, Department of Internal Medicine, and Department of Nephrology, and Dialysis Unit

Kayseri, Turkey (Türkiye)

Outcomes

Primary Outcomes

Blood values

Serum levels of calcium, phosphorus, parathyroid hormone, albumin, hemoglobin, BUN, creatinine, and dialysate calcium

Time frame: At the enrollment

Data from ClinicalTrials.gov

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