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Effect of Calcitriol on Microalbuminuria in Diabetes Patients

Effect of Calcitriol on Microalbuminuria in Diabetes Mellitus type 2

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016091429812N1
Enrollment
60
Registered
2017-02-27
Start date
2015-03-21
Completion date
Unknown
Last updated
2019-05-21

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

Conditions

Diabetic nephropathy. Glomerular disorders in diabetes mellitus

Interventions

Intervention 1: Calcitriol 0.25 mcg administered for 3 months for patients in intervention group. Intervention 2: placebo.

Sponsors

Vice Chancellor for Research of University of Medical Sciences and Health Services,Yazd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Type 2 diabetes concumption of ARB and ACE inhibitors for at least one year However, despite the above treatment, microalbuminuria still exists (30-300 mg of albumin after 8-12 hours of fasting, which is checked by the turbidimetry method)

Exclusion criteria

Exclusion criteria: type 1 diabetes blood pressure> 140/90 PTH>75 ng/d history of kidney stones or kidney stones during the study period hypercalcemi ( Ca > 10/3 mg/dl) calcitriol use or vitamin D albuminuria >300 mg/24hours acute liver disease

Design outcomes

Primary

MeasureTime frame
Mico-albuminuria. Timepoint: at baseline and three months after the initiation of trial. Method of measurement: Blood sampling.;Fbs. Timepoint: at baseline and three months after the initiation of trial. Method of measurement: Blood sampling.;HbA1c. Timepoint: at baseline and three months after the initiation of trial. Method of measurement: Blood sampling.;TG. Timepoint: at baseline and three months after the initiation of trial. Method of measurement: Blood sampling.;Total cholestrol. Timepoint: at baseline and three months after the initiation of trial. Method of measurement: Blood sampling.;LDL. Timepoint: at baseline and three months after the initiation of trial. Method of measurement: Blood sampling.;HDL. Timepoint: at baseline and three months after the initiation of trial. Method of measurement: Blood sampling.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHemayati Roya

Yazd Diabetes Research Center

hemayatiroya@yahoo.com+98 35 3728 0215

Outcome results

None listed

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