Multiclinic controlled trial of diltiazem for Prinzmetal's angina.

Abstract

To assess the efficacy of a new calcium entry blocker, diltiazem (Cardizem), for prophylaxis of Prinzmetal's angina, 48 patients were studied in randomized, multiple crossover multiclinic study (2 weeks single-blind, 8 weeks double-blind). Diltiazem dosage in one crossover phase was 120 mg per day; in the other, 240 mg per day. Therapeutic response was measured by patients' diary records of angina frequency and nitroglycerin tablet consumption. Treatment with 120 mg of diltiazem per day reduced angina by 41 percent from the entry placebo period and 20 percent from the paired placebo period (p less than 0.005). Treatment with 240 mg of diltiazem per day reduced angina frequency by 68 percent from the entry placebo period and 43 percent from the paired placebo period (p less than 0.01). There were similar reductions in nitroglycerin consumption. Adverse experiences that may have been related to the medication were noted in only 5 percent of patients. There were no alterations in blood pressure or heart rate. The PR interval increased 3 percent at the 240 mg dosage level. We conclude that diltiazem is an effective and safe agent for control of symptoms of Prinzmetal's angina.

• Authors: J S Schroeder, R L Feldman, T D Giles, M J Friedman, A N DeMaria, E L Kinney, S M Mallon, B Pit, R Meyer, L L Basta, R C Curry Jr, B M Groves, R N MacAlpin
• Journal: The American journal of medicine (Am J Med) Vol. 72 Issue 2 Pg. 227-32 (Feb 1982) ISSN: 0002-9343 [Print] United States
• PMID: 7036726 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)

Chemical References

• Benzazepines
• Diltiazem

Topics

• Adult
• Aged
• Angina Pectoris, Variant (drug therapy)
• Benzazepines (therapeutic use)
• Clinical Trials as Topic
• Coronary Vasospasm (drug therapy)
• Diltiazem (adverse effects, therapeutic use)
• Double-Blind Method
• Female
• Heart Conduction System (drug effects)
• Humans
• Male
• Middle Aged