The Role of FGF23 and Asymmetric Dimethylarginine (ADMA) in Chronic Kidney Disease
1 other identifier
observational
100
1 country
1
Brief Summary
In chronic kidney disease calcium (Ca) and phosphate (P) metabolism disorders are very common and also they are one of the leading causes of morbidity in these population. FGF23 is a novel factor that contributes Ca-P disorders. It has been hypothesized that FGF 23 increase is mediated by asymmetric dimethylarginine (ADMA). The aim of the study is to evaluate this hypothesis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2011
CompletedFirst Submitted
Initial submission to the registry
March 16, 2011
CompletedFirst Posted
Study publicly available on registry
March 17, 2011
CompletedMarch 17, 2011
March 1, 2011
March 16, 2011
March 16, 2011
Conditions
Keywords
Study Arms (3)
Group I
Stage 2 Non-diabetic Chronic Kidney Disease
Group II
Stage 3 Non-diabetic Chronic Kidney Disease
Group III
Stage 4 Non-diabetic Chronic Kidney Disease
Eligibility Criteria
Stage 2-4 Non-diabetic Chronic Kidney Disease patients
You may qualify if:
- between ages of 18 - 65 years old
- chronic kidney disease of stage 2-4
You may not qualify if:
- presence of diabetes mellitus or ischemic hearth disease
- taking vitamin d therapy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ankara Education and Research Hospital
Ankara, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Sponsor Type
- OTHER GOV
Study Record Dates
First Submitted
March 16, 2011
First Posted
March 17, 2011
Study Start
March 1, 2011
Last Updated
March 17, 2011
Record last verified: 2011-03