NCT Number: NCT00362960
Olmesartan Medoxomil and Diabetic Nephropathy
Evaluation of several olmesartan dosages compared to losartan on proteinuria, renal function and inflammatory markers in patients with diabetic nephropathy
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Notify MeKey information
Conditions
Age range
30 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Frýdlant, Czechia
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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 tolerability or inefficacy of previous treatment, or verification that treatment is still necessary
Exclusion criteria
- Females pregnant, nursing or planning to become pregnant or were of childbearing potential and not using acceptable methods of contraception
- Secondary forms of hypertension other than diabetic nephropathy, malignant hypertension 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 hepatic disease or myocardial infarction in last 12 months or a previous history of any serious underlying disease
- Concurrent renal disease, nephrectomy and/or renal transplant, serum creatinine level greater 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 have influenced BP
- History of hypersensitivity, lack of response or contraindication to Ang II-antagonists, HCTZ or atenolol, or hypersensitivity to related drugs (cross-allergy)
Treatment and study plan
Losartan
DrugPrimary outcomes
-
Efficacy of olmesartan medoxomil doses compared to losartan in
-
patients with type 2 diabetes and nephropathy in terms of the change in
-
proteinuria (total urinary protein excretion) from baseline.
Secondary outcomes
-
Efficacy of the treatment with olmesartan medoxomil dosages compared to
-
losartan in patients with type 2 diabetes and nephropathy in terms of
-
change in:
-
creatinine clearance (CLCR)
-
the protein pattern (nephelometry)
-
inflammatory markers (circulating serum markers).
-
Evaluate safety and tolerability of all treatments.
Sponsors and collaborators
Lead sponsor
Sankyo Pharma Gmbh
Industry
Registry information
Official study title
Effect of Different Doses of Olmesartan Medoxomil Compared to Losartan on Proteinuria, Renal Function and Inflammatory Markers in Type 2 Diabetics With Nephropathy
Important dates
- Study start
- 2003
- Study completion
- 2004
- First posted
- Aug 15, 2006
- Registry last updated
- Oct 9, 2006
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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