Patients with ESRD undergoing hemodialysis. Hypertensive chronic kidney disease with stage 5 chronic kidney disease or end stage renal disease
Conditions
Interventions
Intervention 1: Intervention group: Calcium-D capsule (Shefa company contains 500 mg calcium and 200 IU vitamin D) along with vitamin K2 tablets (capsule containing vitamin K2-7, microcrystalline, cel
Sponsors
Gorgan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Not using anticoagulant drugs age 18-75 years patient with ESRD and hemodialysis patients that dialyses > 1 months.
Exclusion criteria
Exclusion criteria: Coagulation disorder Lack of consent to study Hypocalcemia or hypercalcemia in patients Infection before and during treatment with High CRP Using of antibiotic drugs Using of osteoporosis drugs lack of medication compliance
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of the average serum levels of albumin after the implementation of the intervention. Timepoint: At the beginning of the study and 3 month later. Method of measurement: blood sample.;Comparison of the average serum levels of calcium after the implementation of the intervention. Timepoint: At the beginning of the study and 3 month later. Method of measurement: blood sample.;Comparison of the average serum levels of phosphorus after the implementation of the intervention. Timepoint: At the beginning of the study and 3 month later. Method of measurement: blood sample.;Comparison of the average serum levels of Vitamin D after the implementation of the intervention. Timepoint: At the beginning of the study and 3 month later. Method of measurement: blood sample. | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of the mean serum PTH level after the implementation of the intervention to the basic value. Timepoint: At the beginning of the study and 3 month later. Method of measurement: blood sample.;Comparison of the mean serum alkaline phosphatase (AKP) level after the implementation of the intervention to the basic value. Timepoint: At the beginning of the study and 3 month later. Method of measurement: blood sample. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSedighe Maghsoudloo
Gorgan University of Medical Sciences
Outcome results
None listed