Olmesartan Medoxomil and Diabetic Nephropathy

Last updated: October 6, 2006
Sponsor: Sankyo Pharma Gmbh
Overall Status: Completed

Phase

3

Condition

Diabetes Mellitus, Type 2

Renal Failure

Kidney Failure

Treatment

N/A

Clinical Study ID

NCT00362960
SE-866/29
  • Ages > 30
  • All Genders

Study Summary

Evaluation of several olmesartan dosages compared to losartan on proteinuria, renal function and inflammatory markers in patients with diabetic nephropathy

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Male or female European out-patients

  • Greater than or equal to 30 years of age

  • Type 2 diabetes first diagnosed at greater than or equal to 30 years of age

  • Urinary protein excretion between 200-4000 mg/day exclusive

  • Mean sitting dBP less than or equal to 110 mgHg

  • Medically justifiable to withdraw antihypertensive treatment due to poor tolerabilityor inefficacy of previous treatment, or verification that treatment is still necessary

Exclusion

Exclusion Criteria:

  • Females pregnant, nursing or planning to become pregnant or were of childbearingpotential and not using acceptable methods of contraception

  • Secondary forms of hypertension other than diabetic nephropathy, malignanthypertension or patients with sitting dBP exceeding 110 mmHg or sitting sBP exceeding 200 mmHg

  • ECG evidence of 2nd or 3rd degree AV-block, atrial fibrillation, cardiac arrhythmia (requiring therapy) or bradycardia

  • Presence of significant cardiovascular disease

  • Significant cerebrovascular disease, gastrointestinal, haematological or hepaticdisease or myocardial infarction in last 12 months or a previous history of anyserious underlying disease

  • Concurrent renal disease, nephrectomy and/or renal transplant, serum creatinine levelgreater than or equal to 2.0 mg/dL or creatinine clearance CLCR less than or equal to 50 mL/min

  • Clinically significant lab abnormalities (ASAT/SGOT, ALAT/SGPT and γ-GT )

  • Serum potassium level < 2.5 mmol/L or > 5.5 mmol/L

  • Treatment of concurrent indications with drugs or medication which could haveinfluenced BP

  • History of hypersensitivity, lack of response or contraindication to AngII-antagonists, HCTZ or atenolol, or hypersensitivity to related drugs (cross-allergy)

Study Design

Total Participants: 300
Study Start date:
May 01, 2003
Estimated Completion Date:
September 30, 2004

Connect with a study center

  • Frydlant v Cechach,
    Czech Republic

    Site Not Available

  • Liberec,
    Czech Republic

    Site Not Available

  • Prague,
    Czech Republic

    Site Not Available

  • Tartu,
    Estonia

    Site Not Available

  • Augsburg,
    Germany

    Site Not Available

  • Greifenstein-Beilstein,
    Germany

    Site Not Available

  • Hannover,
    Germany

    Site Not Available

  • Zwijndrecht,
    Netherlands

    Site Not Available

  • Grodzisk Mazowiecki,
    Poland

    Site Not Available

  • Krakow,
    Poland

    Site Not Available

  • Plock,
    Poland

    Site Not Available

  • Poznan,
    Poland

    Site Not Available

  • Pruszkow,
    Poland

    Site Not Available

  • Torun,
    Poland

    Site Not Available

  • Warsaw,
    Poland

    Site Not Available

  • Watlack,
    Poland

    Site Not Available

  • Wolomin,
    Poland

    Site Not Available

  • Wroclaw,
    Poland

    Site Not Available

  • Banska Bystrica,
    Slovakia

    Site Not Available

  • Kosice,
    Slovakia

    Site Not Available

  • Lucenec,
    Slovakia

    Site Not Available

  • Martin,
    Slovakia

    Site Not Available

  • Nitra,
    Slovakia

    Site Not Available

  • Nove Zamky,
    Slovakia

    Site Not Available

  • Sahy,
    Slovakia

    Site Not Available

  • Barcelona,
    Spain

    Site Not Available

  • Madrid,
    Spain

    Site Not Available

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