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Last Updated: November 22, 2024

CLINICAL TRIALS PROFILE FOR LISINOPRIL


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All Clinical Trials for lisinopril

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00000542 ↗ Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) Completed National Heart, Lung, and Blood Institute (NHLBI) Phase 3 1993-08-01 To determine if the combined incidence of nonfatal myocardial infarction and coronary heart disease death differs between diuretic-based and each of three alternative antihypertensive pharmacological treatments. Also, to determine, in a subset of this population, if lowering serum cholesterol with a HMG CoA reductase inhibitor in older adults reduces all-cause mortality compared to a control group receiving usual care. Conducted in conjunction with the Department of Veterans' Affairs.
NCT00004266 ↗ Drugs for High Blood Pressure and High Cholesterol in American Indians With Type 2 Diabetes Completed Hennepin County Medical Center, Minneapolis Phase 3 1993-08-01 OBJECTIVES: I. Establish a long-term working relationship between clinical investigators and the Minnesota American Indian community. II. Compare the effectiveness of lisinopril (an angiotensin-converting enzyme inhibitor) and nifedipine (a calcium channel blocker) in preventing nephropathy and vascular disease in Minnesota American Indians with non-insulin-dependent diabetes mellitus and microalbuminuria. III. Compare the effectiveness of simvastatin (a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor) with lipid-lowering strategies recommended by the National Cholesterol Education Program in preventing nephropathy and vascular diseases in these patients.
NCT00004266 ↗ Drugs for High Blood Pressure and High Cholesterol in American Indians With Type 2 Diabetes Completed National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Phase 3 1993-08-01 OBJECTIVES: I. Establish a long-term working relationship between clinical investigators and the Minnesota American Indian community. II. Compare the effectiveness of lisinopril (an angiotensin-converting enzyme inhibitor) and nifedipine (a calcium channel blocker) in preventing nephropathy and vascular disease in Minnesota American Indians with non-insulin-dependent diabetes mellitus and microalbuminuria. III. Compare the effectiveness of simvastatin (a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor) with lipid-lowering strategies recommended by the National Cholesterol Education Program in preventing nephropathy and vascular diseases in these patients.
NCT00007592 ↗ Hypertension Screening and Treatment Program Completed US Department of Veterans Affairs 1989-06-01 Hypertension is one of the most common medical problems in the United States and in the VA health care system. It has been well-documented that hypertension can be effectively treated. However, there remain important unresolved clinical questions in the area of antihypertensive treatment. For example, how much is mortality affected by visit compliance, blood pressure control and type of antihypertensive agent? Or, are some regimens associated with more morbidity than others? Or, are there inexpensive regimens that are as effective as more expensive regimens? The amount of data that is available from this demonstration project (currently 6,100 patients) will help address these questions. The answers to these questions should result in better care for veterans with hypertension.
NCT00007592 ↗ Hypertension Screening and Treatment Program Completed VA Office of Research and Development 1989-06-01 Hypertension is one of the most common medical problems in the United States and in the VA health care system. It has been well-documented that hypertension can be effectively treated. However, there remain important unresolved clinical questions in the area of antihypertensive treatment. For example, how much is mortality affected by visit compliance, blood pressure control and type of antihypertensive agent? Or, are some regimens associated with more morbidity than others? Or, are there inexpensive regimens that are as effective as more expensive regimens? The amount of data that is available from this demonstration project (currently 6,100 patients) will help address these questions. The answers to these questions should result in better care for veterans with hypertension.
NCT00067977 ↗ HALT Progression of Polycystic Kidney Disease Study B Completed Boehringer Ingelheim Phase 3 2006-01-01 The efficacy of interruption of the renin-angiotensin-aldosterone system (RAAS) on the progression of cystic disease and on the decline in renal function in autosomal dominant kidney disease (ADPKD) will be assessed in two simultaneous multicenter randomized clinical trials targeting different levels of kidney function: 1) early disease defined by GFR >60 mL/min/1.73 m2 (Study A); and 2) moderately advanced disease defined by GFR 25-60 mL/min/1.73 m2 (Study B). Participants will be recruited and enrolled, either to Study A or B, over the first three years. Participants enrolled in Study B will be followed for five-to-eight years, with the average length of follow-up being six and a half years. Combination therapy will use angiotensin-converting-enzyme inhibitor (ACE-I) and an angiotensin-receptor blocker (ARB). Monotherapy will use ACE-I alone.
NCT00067977 ↗ HALT Progression of Polycystic Kidney Disease Study B Completed Merck Sharp & Dohme Corp. Phase 3 2006-01-01 The efficacy of interruption of the renin-angiotensin-aldosterone system (RAAS) on the progression of cystic disease and on the decline in renal function in autosomal dominant kidney disease (ADPKD) will be assessed in two simultaneous multicenter randomized clinical trials targeting different levels of kidney function: 1) early disease defined by GFR >60 mL/min/1.73 m2 (Study A); and 2) moderately advanced disease defined by GFR 25-60 mL/min/1.73 m2 (Study B). Participants will be recruited and enrolled, either to Study A or B, over the first three years. Participants enrolled in Study B will be followed for five-to-eight years, with the average length of follow-up being six and a half years. Combination therapy will use angiotensin-converting-enzyme inhibitor (ACE-I) and an angiotensin-receptor blocker (ARB). Monotherapy will use ACE-I alone.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for lisinopril

Condition Name

Condition Name for lisinopril
Intervention Trials
Hypertension 45
Cardiovascular Disease 6
Healthy 6
Diabetic Nephropathy 5
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Condition MeSH

Condition MeSH for lisinopril
Intervention Trials
Hypertension 49
Kidney Diseases 17
Cardiovascular Diseases 10
Diabetes Mellitus 9
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Clinical Trial Locations for lisinopril

Trials by Country

Trials by Country for lisinopril
Location Trials
United States 436
Canada 8
Spain 6
Puerto Rico 6
Italy 5
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Trials by US State

Trials by US State for lisinopril
Location Trials
Texas 24
Ohio 21
California 21
New York 20
Minnesota 18
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Clinical Trial Progress for lisinopril

Clinical Trial Phase

Clinical Trial Phase for lisinopril
Clinical Trial Phase Trials
Phase 4 31
Phase 3 24
Phase 2/Phase 3 2
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Clinical Trial Status

Clinical Trial Status for lisinopril
Clinical Trial Phase Trials
Completed 82
Terminated 12
Recruiting 12
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Clinical Trial Sponsors for lisinopril

Sponsor Name

Sponsor Name for lisinopril
Sponsor Trials
GlaxoSmithKline 14
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) 9
Novartis 7
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Sponsor Type

Sponsor Type for lisinopril
Sponsor Trials
Other 130
Industry 63
NIH 22
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