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首页> 外文期刊>Clinical therapeutics >Tramadol/Acetaminophen combination tablets for the treatment of chronic lower back pain: A multicenter, randomized, double-blind, placebo-controlled outpatient study.
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Tramadol/Acetaminophen combination tablets for the treatment of chronic lower back pain: A multicenter, randomized, double-blind, placebo-controlled outpatient study.

机译:曲马多/对乙酰氨基酚联合治疗慢性下腰痛的片剂:一项多中心,随机,双盲,安慰剂对照的门诊研究。

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BACKGROUND: Tramadol and acetaminophen (APAP) have both shown efficacy in the treatment of lower back pain. The combination of these 2 agents has demonstrated synergistic analgesic action in animal models at specific ratios.OBJECTIVE: This study assessed the long-term (3-month) efficacy and safety of tramadol 37.5 mg/APAP 325 mg combination tablets in the treatment of chronic lower back pain.METHODS: Patients with at least moderate lower back pain (pain visual analog [PVA] score >/=40 mm on a 100-mm scale) were randomized to receive up to 8 tablets of tramadol/APAP per day or placebo for 91 days. Medication was titrated from 1 to 4 tablets/d by day 10. The primary efficacy measure was PVA score at the final visit. Secondary measures included scores on the Pain Relief Rating Scale (PRRS), Short-Form McGill Pain Questionnaire (SF-MPQ), Roland Disability Questionnaire (RDQ), and 36-Item Short-Form Health Survey (SF-36); the incidence of discontinuation due to insufficient pain relief (Kaplan-Meier analysis); and overall assessments of medication by the patients and investigators.RESULTS: Three hundred eighteen patients (161 tramadol/APAP, 157 placebo) were included in the intent-to-treat population, defined as all patients who took >/=1 dose of study medication and had >/=1 postrandomization efficacy measurement. The mean age of the study population was 53.9 years, 63.2% were female, 90.3% were white, and the mean baseline PVA score was 70.0 mm. There were no significant differences between groups at baseline. Tramadol/APAP significantly improved final PVA scores (P = 0.015) and final PRRS scores (P < 0.001) compared with placebo. Tramadol/APAP also significantly improved RDQ scores (P
机译:背景:曲马多和对乙酰氨基酚(APAP)均已显示出治疗下背部疼痛的功效。这两种药物的组合已证明在动物模型中以特定比例具有协同镇痛作用。目的:本研究评估了37.5 mg / APAP 325 mg曲马多联合片剂在长期治疗中的长期(3个月)疗效和安全性方法:将至少具有中度下腰痛(疼痛视觉类似物[PVA]评分> / = 40 mm(以100 mm评分)的患者)随机分组,每天接受多达8片曲马多/ APAP或安慰剂持续91天。到第10天,药物的滴定剂量为1-4片/ d。主要功效指标是最后一次就诊时的PVA评分。次要措施包括疼痛缓解等级量表(PRRS),麦吉尔简短疼痛问卷(SF-MPQ),罗兰残疾问卷(RDQ)和36项简短健康调查(SF-36)的得分;因疼痛缓解不足而中断治疗的发生率(Kaplan-Meier分析);结果:意向治疗人群中包括38例患者(161曲马多/ APAP,157安慰剂),定义为所有接受> / = 1剂量研究的患者药物治疗,并具有> / = 1的随机后功效测量。研究人群的平均年龄为53.9岁,女性为63.2%,白人为90.3%,平均基线PVA评分为70.0 mm。基线时各组之间无显着差异。与安慰剂相比,曲马多/ APAP显着改善了最终PVA评分(P = 0.015)和PRRS最终评分(P <0.001)。曲马多/ APAP还显着改善了RDQ评分(P

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