Key result
Picotamide significantly slowed the progression of early carotid atherosclerotic lesions, resulting in lower mean percent stenosis (26% vs 35%, P<0.01) compared to placebo at 24 months.
Why the study?
Does picotamide reduce the progression of carotid atherosclerotic lesions in type II diabetic patients with asymptomatic mild or moderate nonstenotic carotid lesions?
RCT (n=50)
Double-blind
Randomized
Does picotamide reduce the progression of carotid atherosclerotic lesions in type II diabetic patients with asymptomatic mild or moderate nonstenotic carotid lesions?
Long-term treatment with picotamide slows the echographic progression of early carotid atherosclerotic lesions in type II diabetic patients compared to placebo.
Answers are grounded in this paper and cite their sources.
Picotamide may slow early carotid lesion progression in type 2 diabetes; extends RCT evidence for targeted antiplatelet therapy in diabetic atherosclerosis.
BACKGROUND AND PURPOSE: We assessed the effects of long-term treatment with picotamide, an antiplatelet agent with dual antithromboxane activity, on the evolution of early asymptomatic carotid atherosclerotic lesions in diabetic patients. METHODS: In a double-blind, placebo-controlled, 2-year study, 50 type II normotensive diabetic patients (35 men; mean age, 66 +/- 5 years) with asymptomatic mild or moderate nonstenotic (< 50%) carotid atherosclerotic lesions and negative history of cerebrovascular ischemic events were enrolled and randomly given picotamide (300 mg TID) or the corresponding placebo. A high-resolution, real-time B-scan echographic assessment of carotid arteries was performed at baseline and after 1, 3, 6, 12, 18, and 24 months of double-blind treatment. Prevalence and evolutionary trends of carotid atherosclerotic lesions (number per patient and mean stenosis expressed as percent) were considered as efficacy primary end points. RESULTS: At baseline, mean +/- SD numbers of carotid atherosclerotic lesions per patient were 2.7 +/- 1.8 and 2.2 +/- 1.2 in the picotamide and placebo groups, respectively. Mean +/- SD percent stenosis was 25.3 +/- 7% in the picotamide group and 27.3 +/- 6% in the placebo group. Forty-nine patients completed the study. At month 24, the placebo group (n = 24) showed a significant progression in number of carotid atherosclerotic lesions (3.04 +/- 1.8; P < .02 versus baseline) and in mean percent stenosis (35 +/- 17%; 95% confidence interval, 33% to 37%; P < .01 versus baseline). In the picotamide group (n = 25), mean number of carotid atherosclerotic lesions (2.7 +/- 1.6) and percent stenosis (26 +/- 9%; 95% confidence interval, 24.8% to 27.2%) remained unchanged. At month 24, compared with randomized placebo, lesion numbers (P < .03) and percent stenosis (P < .01) in the picotamide group were significantly lower. During the study, 12 patients experienced major or minor ischemic vascular events (9 in the placebo group and 3 in the picotamide group; P = .07). CONCLUSIONS: In diabetic patients compared with patients receiving placebo, long-term treatment with picotamide can slow the evolution of early carotid atherosclerotic lesions, inhibiting progression of plaque number and growth.
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Cocozza et al. (1995) conducted an RCT in Asymptomatic carotid atherosclerotic lesions in type II diabetes (n=50). Picotamide vs. Placebo was evaluated on Prevalence and evolutionary trends of carotid atherosclerotic lesions (number per patient and mean stenosis expressed as percent) (p=<0.01). Picotamide significantly slowed the progression of early carotid atherosclerotic lesions, resulting in lower mean percent stenosis (26% vs 35%, P<0.01) compared to placebo at 24 months.
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