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溴芬酸钠、萘普生钠与安慰剂缓解原发性痛经疼痛的交叉对照比较。

A crossover comparison of bromfenac sodium, naproxen sodium, and placebo for relief of pain from primary dysmenorrhea.

作者信息

Mehlisch D R, Fulmer R I

机构信息

SCIREX Corporation, Austin, TX, USA.

出版信息

J Womens Health. 1997 Feb;6(1):83-92. doi: 10.1089/jwh.1997.6.83.

DOI:10.1089/jwh.1997.6.83
PMID:9065377
Abstract

Single and multiple oral doses of bromfenac sodium (10 or 50 mg) were compared with naproxen sodium (550 mg loading/275 mg repeat doses) for the relief of pain from primary dysmenorrhea in 54 women using a crossover design. Pain intensity and pain relief were assessed over 6 h after the first dose, and global ratings were made at the end of day 1 and on day 2. A single dose of bromfenac 10 or 50 mg was as effective as the loading dose of naproxen sodium (550 mg) in relieving the pain from dysmenorrhea through a 6-h period. All three active treatments were statistically superior (p < 0.001) to placebo for the primary efficacy variables, 3-h and 6-h total pain relief and 3-h and 6-h summed pain intensity difference. All active treatments were statistically superior (p < 0.05) to placebo for the first dose and day 1 global assessments. One or more adverse study events were reported by 13 patients (25%) who received bromfenac 50 mg, 15 (29%) who received bromfenac 10 mg, 20 (38%) who received naproxen sodium, and 19 (37%) who received placebo. There were no clinically significant differences among the treatments in the types of adverse study events. No serious or unexpected adverse study events were reported, and no women withdrew from the study because of an adverse event. Bromfenac sodium (10 mg or 50 mg) is as effective as naproxen sodium (550 mg loading dose/275 mg repeat doses) for relief of pain from dysmenorrhea.

摘要

采用交叉设计,比较了单剂量和多剂量口服溴芬酸钠(10或50毫克)与萘普生钠(550毫克负荷剂量/275毫克重复剂量)对54名原发性痛经女性疼痛的缓解作用。在首剂给药后6小时内评估疼痛强度和疼痛缓解情况,并在第1天结束时和第2天进行总体评分。单剂量10毫克或50毫克的溴芬酸钠在缓解痛经6小时的疼痛方面与萘普生钠的负荷剂量(550毫克)效果相同。对于主要疗效变量,即3小时和6小时的总疼痛缓解以及3小时和6小时的疼痛强度差值总和,所有三种活性治疗在统计学上均优于安慰剂(p<0.001)。对于首剂和第1天的总体评估,所有活性治疗在统计学上均优于安慰剂(p<0.05)。接受50毫克溴芬酸钠的13名患者(25%)、接受10毫克溴芬酸钠的15名患者(29%)、接受萘普生钠的20名患者(38%)以及接受安慰剂的19名患者(37%)报告了一个或多个不良研究事件。各治疗组不良研究事件的类型无临床显著差异。未报告严重或意外的不良研究事件,也没有女性因不良事件退出研究。溴芬酸钠(10毫克或50毫克)在缓解痛经疼痛方面与萘普生钠(550毫克负荷剂量/275毫克重复剂量)效果相同。

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