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The effect of 1.25 dihydroxy vitamin D on IMT, iron indicators changes induced by inflammation and inflammatory biomarkers in patients with chronic kidney disease

The effect of 1.25 dihydroxy vitamin D on IMT, iron indicators changes induced by inflammation and inflammatory biomarkers in patients with chronic kidney disease

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201211106415N3
Enrollment
40
Registered
2013-03-10
Start date
2013-04-04
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Kidney Disease. Chronic kidney disease

Interventions

It is clinical trial without placebo control of 40 subjects between the ages of 45 and 75 years with chronic kidney disease. CKD patients will be confirmed (by physician) at the initial of diagnosis.
Treatment - Drugs

Sponsors

Vice chancellor for research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria:patients with chronic kidney disease; Patient's written consent to participate in the study; CKD patients with hypovitaminosis D (serum level of 25hydroxy vitamin D<30ng/ml); Not taking ferrous sulfate or Intravenous iron therapy; no evidence of iron deficiencyanemia Exclusion Crieteria: -

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
IMT. Timepoint: Before intervention and after intervention (2month of intervention). Method of measurement: Sonography.;Hepcidin. Timepoint: before intervention and after intervention (2month of intervention). Method of measurement: Measuring serum concentration (ng/ml).;Serum 25 hydroxy vitamin D concentration. Timepoint: Before intervention and after intervention (2month of intervention). Method of measurement: Measuring serum concentration (ng/ml).

Secondary

MeasureTime frame
TIBC. Timepoint: Before and after intervention(2 month). Method of measurement: Serum concentration (micro/dl).;Serum iron. Timepoint: Before and after intervention(2 month). Method of measurement: Serum iron concentration (microgr/dl).;Ferritin. Timepoint: Before and after intervention(2 month). Method of measurement: Serum ferritin concentration (ng/ml).;IL6. Timepoint: Before and after intervention(2 month). Method of measurement: Serum IL6 concentration (pg/ml).;Hemoglobin. Timepoint: Before and after intervention(2 month). Method of measurement: Blood hemoglobin concentration (mg/dl).;Homocystein. Timepoint: Before and after intervention(2 month). Method of measurement: Serum homocystein concentration (micromol/l).;Serum PTH. Timepoint: Before and after intervention(2 month). Method of measurement: Serum PTH concenteration (pg/ml).;Serum calcium. Timepoint: Before and after intervention(2 month). Method of measurement: Serum calcium concentration (mg/dl).;Serum phosphorus. Timepoint: Before and after intervention(2 month). Method of measurement: Serum phosphorus concentration (mg/dl).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKatayoun Kadkhodazadeh

Faculty of Health, Tehran University of Medical Sciences

kattyka63@yahoo.com+98 21 4293 3031

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026