Mineral Bone Disorder in Dialysis

NCT ID: NCT07212972

Last Updated: 2025-10-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

167 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-09-25

Study Completion Date

2020-06-20

Brief Summary

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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.

Detailed Description

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Conditions

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

Study Design

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Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Study Groups

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dialysis

167 patients diagnosed with CKD and undergoing HD or PD were included in the study

Hemodialysis or peritoneal Dialysis

Intervention Type OTHER

Hemodialysis or peritoneal Dialysis

Interventions

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Hemodialysis or peritoneal Dialysis

Hemodialysis or peritoneal Dialysis

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Çanakkale Onsekiz Mart University

OTHER

Sponsor Role lead

Responsible Party

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Şeyma Eroğlu

Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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

Kayseri, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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TZ-B

Identifier Type: -

Identifier Source: org_study_id

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