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Effectiveness of oral administration of vitamin D in anemia of patients with type 2 diabetes with mild renal impairment

Effectiveness of oral administration of vitamin D in anemia of patients with type 2 diabetes with mild renal impairment

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016011125951N1
Enrollment
100
Registered
2016-06-14
Start date
2016-03-25
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

anemia.

Interventions

Intervention 1: intervention group: 50 patients in this group receiving 50000 unit per week (pearl, Manufacturing Co. Zahravi) for 8 weeks. Intervention 2: Control group: 50 patients in placebo group
Treatment - Drugs
intervention group: 50 patients in this group receiving 50000 unit per week (pearl, Manufacturing Co. Zahravi) for 8 weeks.
Control group: 50 patients in placebo group receiving placebo (pearl, Manufacturing Co. Zahravi) for 8 weeks.

Sponsors

Vice Chancellor for research of Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: inclusion criteria :all diabetic cases with anemia based on WHO criteria and mild renal impairment according to Staging ( KDIGO 2012 exclusion criteria:history of transfusion during 3 months ago/history of recent bleeding/history of recent infection during 2 months ago/history of supplement therapy/pregnancy/smoking/chronic disease of liver/kidney hypercalcemia/hyperparathyroidesim/explained anemia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hemoglobin and vitamin D before intervention and 8 weeks after interventin. Timepoint: before intervention and at the end of intervention ( end of second month). Method of measurement: enzyme immunoassay method (EIA) [immunodiagnostic system; IDS (LTD), UK].

Secondary

MeasureTime frame
Srum 25 hydroxy vitamin D. Timepoint: 8 WEEKS. Method of measurement: enzyme immunoassay method (EIA).

Countries

Iran (Islamic Republic of)

Contacts

Public Contactseyed mehdi hashemi

seyed mehdi hashemi

hashemimahdi@zaums.ac.ir+98 54 3342 6343

Outcome results

None listed

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