Short- and Long-Term Effects of Molsidomine Retard and Molsidomine Nonretard on Exercise Capacity and Clinical Status in Patients with Stable Angina: A Multicenter Randomized Double-Blind Crossover Placebo-Controlled Trial

A multicenter, randomized, double-blind, crossover, placebo-controlled study was conducted in 90 isosorbide dinitrate responders showing stable angina to compare the efficacy of molsidomine retard, 8 mg b.i.d., with that of molsidomine, 4 mg t.i.d., for 6 weeks. Total work performance (workload × mi...

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Veröffentlicht in:Journal of cardiovascular pharmacology 1998-02, Vol.31 (2), p.271-276
Hauptverfasser: Messin, Roger, Karpov, Youri, Baikova, Natalia, Bruhwyler, Jacques, Monseu, Marie-Joëlle, Guns, Corry, Géczy, Joseph
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Sprache:eng
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Zusammenfassung:A multicenter, randomized, double-blind, crossover, placebo-controlled study was conducted in 90 isosorbide dinitrate responders showing stable angina to compare the efficacy of molsidomine retard, 8 mg b.i.d., with that of molsidomine, 4 mg t.i.d., for 6 weeks. Total work performance (workload × min) was significantly improved, compared with baseline and placebo until 8 and 12 h after molsidomine and molsidomine retard administration, respectively. ST-segment depression decreased significantly under the two treatments at 60 W as well as at maximal exercise. The rate-pressure product (heart rate × systolic blood pressure) decreased and increased significantly at submaximal and maximal exercise level, respectively. All these effects remained significant after 6-week treatment, with only the ST segment showing a nonsignificant tendency to improvement at maximal work. The frequency of anginal attacks and of sublingual nitroderivative-tablets consumption decreased significantly with molsidomine, 4 mg, and molsidomine retard, 8 mg. However, overall results showed that the latter form reduces myocardial ischemia more efficiently at submaximal exercise level, has a more prolonged effect on exercise tolerance, and maintains it at a somewhat higher level after 6-week treatment.
ISSN:0160-2446
1533-4023
DOI:10.1097/00005344-199802000-00013