Nicergoline in mild to moderate dementia. A multicenter, double-blind, placebo-controlled study.

Abstract:

:In view of some controversies still existing about the real efficacy of ergot derivatives in the management of dementia, a double-blind, randomized, parallel group trial extending up to 6 months was carried out to compare the effects of nicergoline, 60 mg daily, and placebo in 315 patients suffering from mild to moderate dementia. Clinical evaluation was performed by the SCAG scale. The trial, which included a 1-month placebo run-in period, showed that both placebo and nicergoline were associated with some degree of improvement. The effect of nicergoline, however, was significantly greater and more sustained, steadily increasing with time. In particular, the difference between nicergoline and placebo in mean total SCAG score was 5.5 at 3 months (95% confidence interval: 3.6-7.4) and increased to 9.8 at 6 months (95% confidence interval: 7.8-11.8). A comparison of nicergoline versus placebo in the frequencies of changes in each item of the SCAG showed also a significant difference at 6 months, the percent of patients displaying an improvement by at least 2 points ranging from 13.5 (bothersome) to 30.2 (disorientation) in nicergoline group, against 4.1 (self-care) to 14.3 (fatigue) in placebo group. The safety of nicergoline, as judged by hemodynamic changes and drug-related adverse reactions, was quite satisfactory.

journal_name

J Am Geriatr Soc

authors

Battaglia A,Bruni G,Ardia A,Sacchetti G

doi

10.1111/j.1532-5415.1989.tb05494.x

subject

Has Abstract

pub_date

1989-04-01 00:00:00

pages

295-302

issue

4

eissn

0002-8614

issn

1532-5415

journal_volume

37

pub_type

临床试验,杂志文章,多中心研究,随机对照试验
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