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Effect of raloxifen on kidney function in post menopausal women with diabetic nephropathy

Effect of raloxifen in post menopausal women with diabetic nephropathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138904151179N4
Enrollment
50
Registered
2011-03-20
Start date
2009-09-23
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

Diabetic Nephropathy.

Interventions

Intervention 1: placebo for 4 months. Intervention 2: Raloxifen tablets 60mg/daily for 4 months.
Placebo
Treatment - Drugs
placebo for 4 months
Raloxifen tablets 60mg/daily for 4 months

Sponsors

Zanjan Metabolic Diseases Research Center, Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria : confirmed menopause (last period of the patient over the past year and FSH levels is more than 25mu/L, Age less than 70 years, confirmed albuminuria due to DM (ACR> 30mg/gr) Exclusion criteria: History of Treatment with estrogen or SERM in the past six months, a personal history of breast or Genicologic cancer, History of thrombotic disorders, GFR less than 30 mL/min, hypertriglyceridemia over than 400 mg/dl, Active liver disease, intolerance to raloxifene or other Allergic reactions

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Albuminuryia. Timepoint: at the begining of the study and 4month after intervention. Method of measurement: Nephelometry.

Secondary

MeasureTime frame
Lipid profile(TG, Cholesterol, HDL-C). Timepoint: at the begining of the study and 4month after intervention. Method of measurement: Enzymatic methods.;Blood pressure. Timepoint: at the begining of the study and 2&4 month after intervention. Method of measurement: standard methods checking for BP.;HbA1c. Timepoint: at the beginning of the study and 4 months after intervention. Method of measurement: lone exchange.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Faranak Sharifi

Zanjan Metabolic Diseases Research Center

faranaksharifi@hotmail.com zmdrc@zums.ac.ir+98 24 1727 0814

Outcome results

None listed

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