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Maximal Dose of Angiotensin Converting Enzyme (ACE) Inhibitor for Treatment of Diabetic Kidney Disease

Information source: Steno Diabetes Center
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Diabetes Mellitus, Type I; Diabetic Nephropathy

Intervention: Lisinopril (Drug)

Phase: N/A

Status: Completed

Sponsored by: Steno Diabetes Center

Official(s) and/or principal investigator(s):
Hans-Henrik Parving, MD, Study Chair, Affiliation: Steno Diabetes Center

Summary

The primary aim is to evaluate the anti proteinuric effect of increasing doses of the ACE inhibitor, lisinopril: 20, 40 and 60 mg daily in type 1 diabetic patients with hypertension and diabetic nephropathy. The secondary aim is to evaluate the effect on blood pressure (24 hour ambulatory blood pressure) and kidney function (glomerular filtration rate (GFR)). The tertiary aim is to evaluate differences in response to treatment according to ACE/insertion/deletion (ID)-genotypes and other genetic variants in the genes of the renin angiotensin system.

Clinical Details

Official title: Optimal Dose of ACE Inhibitor for Treatment of Diabetic Nephropathy in Type 1 Diabetic Patients With Hypertension and Diabetic Nephropathy

Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Prevention

Primary outcome: albuminuria

Secondary outcome:

blood pressure (24 hour ambulatory) and GFR.

Tertiary: differences in response to treatment in patients with different ACE/ID and other renin angiotensin system genotypes.

Detailed description: This is a randomized, double-blind cross-over study with three treatment periods consisting of 20, 40 and 60 mg lisinopril daily in random order. The endpoints of the study will be examined after each treatment period. There is no wash out between treatment periods. To minimize the risk of hypotension every treatment period starts with 20 mg lisinopril for two weeks. Thus, the risk of adverse effects is minimized and an increase in dose from 0 mg to 60 mg lisinopril is avoided. The patients usual antihypertensive treatments will be stopped in a period of 8 weeks (wash out) before randomization. Since diuretic drugs will be needed by almost every patient in the study to avoid oedema all patients will be treated with lasix retard 60 – 120 mg daily. Patients: 60 type 1 diabetic patients with diabetic nephropathy and hypertension (blood pressure > 135 mm Hg systolic and/or 85 mm Hg diastolic). Methods: The endpoints of the study will be examined at baseline and after each treatment period corresponding to 8, 16, and 24 weeks after randomization. The following parameters are determined after each treatment period: Albuminuria (determined from three consecutive 24 hours urine collections), kidney function (GFR – by plasma clearance of 51Cr-EDTA ), and 24 hour ambulatory blood pressure (TM-2420/2421). Furthermore, the concentrations of TGF-ß, sodium, creatinine, and carbamide in the 24 hour urinary samples are determined. The plasma concentration of albumin, renin, angiotensin II, and aldosterone is measured. DNA is extracted from a blood sample and genetic variants in the renin-angiotensin system are measured including the ACE/ID genotype. Endpoints: Primary endpoint: albuminuria ; Secondary endpoints: blood pressure (24 hour ambulatory) and GFR; Tertiary: differences in response to treatment in patients with different ACE/ID and other renin angiotensin system genotypes.

Eligibility

Minimum age: 18 Years. Maximum age: 70 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Type 1 diabetes (WHO criteria)

- Diabetic nephropathy (2 out of 3 consecutive 24 hour urinary samples with albumin

excretion > 300 mg/24hour and diabetic retinopathy in the absence of signs of other kidney or urinary tract disease) 27 or diabetic glomerulosclerosis verified by biopsy.

- Hypertension: Blood pressure > 135 mmHg systolic and/or 85 mm Hg diastolic

repeatedly.

- Age from 18 to 70 years.

Exclusion Criteria:

- Age < 18 years or > 70 years.

- Pregnancy or fertile women not using adequate anticonceptive (intrauterine device,

sterilization, or oral anticonceptive)

- Malignant hypertension.

- Blood pressure > 180/105 mm Hg

- Known renal artery stenosis

- GFR < 30 ml/min/1. 73 m²

- Serum potassium > 4. 8 mmol/ l

- Heart failure, myocardial infarction, unstable angina or coronary bypass operation

within the previous three months.

- Abuse of drugs or alcohol.

- Not able to understand the written information.

- Known intolerance to ACE inhibitors.

- Chronic use of non steroid inflammatory drugs or aspirin (above 1 g/day)

Locations and Contacts

Steno Diabetes Center, Gentofte 2820, Denmark
Additional Information

Starting date: March 2005
Last updated: November 22, 2006

Page last updated: August 23, 2015

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