pathology | Demonstrated benefit and harm | k | | | |
---|
acute myocardial infarction | versus placebo or control No demonstrated result for efficacy | 1 trial | meta-analysis | | Trial | control | p<0.05 | harm | NS |
---|
| fosinopril vs placebo | | | |
Trial | Treatments | Patients | Method |
---|
FAMIS, 1998 | fosinopril (n=142) vs. placebo (n=143) | patients with anterior acute myocardial infarction within 9 hours of onset | double blind Parallel groups Sample size: 142/143 Primary endpoint: LV volumes FU duration: 2 years |
|
heart failure | versus placebo or no treatment No demonstrated result for efficacy | 2 trials | meta-analysis | | Trial | control | p<0.05 | harm | NS |
---|
| fosinopril vs placebo | | | | | fosinopril vs placebo | | | |
Trial | Treatments | Patients | Method |
---|
Brown, 1995 | fosinopril 10 or 20 mg/day (n=116) vs. placebo (n=125) | patients with chronic congestive heart failure (NYHA II-III) not taking digitalis | double blind Sample size: 116/125 Primary endpoint: exercise tolerance FU duration: 24 weeks | FEST (Erhardt), 1996 | fosinopril 40 mg once daily titrated (n=155) vs. placebo (n=153) | patients with mild to moderately severe heart failure (NYHA II-III) | double blind Sample size: 155/153 Primary endpoint: maximal bicycle exercise time FU duration: 12 weeks |
|
hypertension | versus placebo or control No demonstrated result for efficacy | 1 trial | meta-analysis | | Trial | control | p<0.05 | harm | NS |
---|
Zannad et al, 2006 | fosinopril vs placebo | | | all cause mortality 1.09 [0.78; 1.52] Cardiovascular mortality 1.06 [0.67; 1.68] cardiovascular event 1.15 [0.86; 1.53] |
Trial | Treatments | Patients | Method |
---|
Zannad et al, 2006 | Fosinopril 20 mg/day (n=196) vs. matched placebo (n=201) | chronic hemodialysis patients. | double blind Sample size: 196/201 Primary endpoint: FU duration: 24 months |
|