Delapril and Manidipine for Nephroprotection in Diabetes (DEMAND)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00157586
Recruitment Status : Completed
First Posted : September 12, 2005
Last Update Posted : April 9, 2015
Information provided by:
Mario Negri Institute for Pharmacological Research

Brief Summary:
Diabetes mellitus is one of the most common diseases globally, and is considered epidemic in many developed and newly industrialized nations. Diabetes mellitus represents the single largest cause of end-stage renal disease in the U.S. and Europe. At the same time, the primary cause of early death in diabetic patients are cardiovascular complications. Experimental and clinical studies found that angiotensin converting enzyme inhibitors (ACEi) and calcium channel blockers (CCBs) have a specific renoprotective effect and that this effect can be magnified when the two drugs are used in combination. To formally test this hypothesis we designed the Delapril and Manidipine for Nephroprotection in Diabetes (DEMAND) study, a prospective, randomized, double blind trial aimed to compare the effect of 3 years treatment with the ACEi Delapril (30 mg/day), alone or combined to the CCB Manidipine (10 mg/day), versus conventional (non ACEi, non CCB) therapy on the rate of renal function loss and on the incidence of major cardiovascular events in 342 normo- and micro-albuminuric hypertensive type 2 diabetic patients.

Condition or disease Intervention/treatment Phase
Type 2 Diabetes Drug: Delapril, Delapril-Manidipine Fixed combination Phase 3

Detailed Description:

INTRODUCTION Optimal blood pressure, glycemic and lipid control are of utmost importance to minimize the incidence and the progression of chronic renal and cardiovascular complications in patients with diabetes mellitus type 2. Whether angiotensin converting enzyme (ACE) inhibitors alone or combined to calcium channel blockers (CCB) may further reduce the incidence and progression of chronic complications is worth investigating.

AIMS The primary aim of this study is to assess whether at comparable levels of optimal blood pressure and metabolic control, the ACE inhibitor delapril alone or in combination with the dihydropyridine CCB manidipine slow the rate of glomerular filtration rate (GFR) decline as compared with placebo plus conventional antihypertensive therapy in patients with diabetes mellitus type 2 and hypertension. The secondary aim of this study is to assess the effects of delapril and manidipine on the incidence of major cardiovascular events (acute myocardial infarction, ictus or stroke, heart failure requiring hospitalization, revascularization, amputation and cardiovascular mortality).

STUDY POPULATION 342 hypertensive type 2 diabetes patients with normo- or micro-albuminuria. STUDY DESIGN This is a multicenter, prospective, randomized, double-blind, placebo-controlled study. After a 12-week baseline period in which prohibited antihypertensive treatments (ACE inhibitors, angiotensin II receptor antagonists or dihydropyridine calcium channel blockers) will be discontinued, patients will be stratified according to their urinary albumin excretion rate in normo- and micro-albuminuric and then randomized to delapril alone (30 mg/day), delapril (30 mg/day) combined with manidipine (10 mg/day) or placebo given once daily in the morning for at least three years. During the study, systolic and diastolic blood pressure in all treatments groups will be maintained ≤ 120 and 80 mmHg respectively, with fixed doses of study treatments and flexible doses of permitted antihypertensive therapy (diuretics, beta blockers, alfa blockers, centrally acting adrenergic blockers. Blood pressure, blood glucose concentrations and urinary albumin excretion rate will be monitored every three months. Serum lipid concentrations and GFR (estimated with the iohexol plasma clearance) will be measured every six months.

Primary and Secondary Variables. The primary efficacy variable of this study is the rate of GFR decline. The secondary efficacy variable will be the incidence of major cardiovascular events (acute myocardial infarction, ictus or stroke, heart failure requiring hospitalization, revascularization, amputation and cardiovascular mortality).

Study Type : Interventional  (Clinical Trial)
Enrollment : 342 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Diagnostic
Official Title: A Multicenter, Randomized, Prospective, Double-blind Study to Evaluate the Nephroprotective Effect of Delapril Alone or Combined With Manidipine in Patients With Type 2 Diabetes
Study Start Date : February 2002
Study Completion Date : June 2008

Resource links provided by the National Library of Medicine

Primary Outcome Measures :
  1. The rate of decline of glomerular filtration rate (GFR).GFR is measured at baseline,and at 6,12,18,24,30 and 36 months after randomization

Secondary Outcome Measures :
  1. Major cardiovascular events

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   40 Years to 75 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Age ≥ 40 years
  • History of diabetes mellitus type 2 for at least three months with stable antidiabetic treatment
  • Systolic and/or diastolic blood pressure ≥ 135 or 85 mmHg, respectively. In alternative, antihypertensive therapy regardless of blood pressure values
  • Serum creatinine ≤ 1.5 mg/dL
  • Urinary albumin excretion rate < 200 µg/min
  • Written informed consent for the trial participation.

Exclusion Criteria:

  • Clinical or histological evidence of non-diabetic renal disease, including vascular disease of the kidney, obstructive uropathy, prostatic hypertrophy or incomplete bladder emptying
  • Transplanted kidney
  • Moderate to severe chronic heart failure (III-IV stage according to the NYHA classification).
  • Cerebral hemorrhage, stroke or transient ischemic attack within three months prior to the trial enrolment
  • Myocardial infarction within three months prior to the trial enrolment
  • Unstable angina pectoris
  • Mitral valve stenosis, aortic stenosis or hypertrophic cardiomyopathy
  • Secondary (e.g., Cushing disease, phaeochromocytoma, etc.) or severe refractory hypertension
  • Poor glycemic control (HbA1c>11%)
  • Connective tissue or autoimmune disease
  • Hereditary angioneurotic edema
  • Clinically relevant electrolyte imbalance (e.g., serum potassium > 5.5 mmol/L)
  • Clinically relevant hematological disorders
  • Anemia with hemoglobin concentrations < 10 g/dL
  • Serious hepatic disease
  • Pregnancy or lactating or planning a pregnancy
  • Women of childbearing potential without following a scientifically accepted form of contraception
  • Any other serious or terminal concomitant disease
  • Any condition which may interfere with the absorption of the study treatments
  • Any concomitant treatment with ACE inhibitors, angiotensin II blockers, calcium channel blockers, potassium sparing diuretics
  • Chronic treatment with nonsteroidal antiinflammatory drugs, antidepressants and neuroleptics, lithium, cimetidine, immunosuppressive and/or antineoplastic drugs, chronic systemic glucocorticoid therapy more than 7 consecutive days in one month, antiarrhythmic drugs (e.g., chinidin, procainamide), anesthetics/narcotics
  • History of hypersensitivity to delapril or other ACE inhibitors, manidipine or other dihydropyridine CCBs
  • Legal incapacity and/or other circumstances rendering the patient unable to understand the nature, scope and possible consequences of the trial
  • Evidence of an uncooperative attitude
  • Any evidence that allows predicting that the patient will not be able to complete the trial follow-up.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00157586

ASL of Ponte San Pietro - Diabetologic Unit
Ponte San Pietro, Bergamo, Italy, 24036
Clinical Research Center for Rare Diseases
Ranica, Bergamo, Italy, 24020
Hospital of Romano di Lombardia - Diabetologic Unit
Romano di Lombardia, Bergamo, Italy, 24058
Hospital " Bolognini " - Medicine Unit
Seriate, Bergamo, Italy, 24068
Hospital " Treviglio Caravaggio" - Diabetologic Unit
Treviglio, Bergamo, Italy, 24128
Humanitas Institute - Endocrinology and Diabetologic Unit
Rozzano, Milano, Italy, 20089
Hospital "Ospedali Riuniti di Bergamo" - Diabetologic Unit
Bergamo, Italy, 24128
Department of Endocrinolgy, Diabetes and Metabolic Disease - University Medical Center
Lubiana, Slovenia
Sponsors and Collaborators
Mario Negri Institute for Pharmacological Research
Principal Investigator: Piero Ruggenenti, MD Mario Negri Institute

Publications automatically indexed to this study by Identifier (NCT Number): Identifier: NCT00157586     History of Changes
Other Study ID Numbers: DM/PR/7401/005/00
First Posted: September 12, 2005    Key Record Dates
Last Update Posted: April 9, 2015
Last Verified: March 2006

Additional relevant MeSH terms:
Diabetes Mellitus
Diabetes Mellitus, Type 2
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Antihypertensive Agents
Calcium Channel Blockers
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Angiotensin-Converting Enzyme Inhibitors
Protease Inhibitors
Enzyme Inhibitors