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首页> 外文期刊>American journal of therapeutics >A Double-Blind Controlled Trial of a Single Dose Naproxen and an Amino Acid Medical Food Theramine for the Treatment of Low Back Pain
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A Double-Blind Controlled Trial of a Single Dose Naproxen and an Amino Acid Medical Food Theramine for the Treatment of Low Back Pain

机译:单剂量萘普生和氨基酸药物食品Theramine治疗腰痛的双盲对照试验

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To study the safety and efficacy of a new medical food (Theramine) in the treatment of low back pain, we performed a 28-day double-blind randomized controlled trial in 129 patients. Back pain was present for at least 6 weeks and was not mild. Patients were randomly assigned to receive medical food alone (n = 43), naproxen alone (250 mg/d, n = 42), or both medical food and naproxen (n = 44). All patients were assessed by using Roland-Morris Disability Questionnaire, Oswestry Low Back Pain Scale, Visual Analog Scale Evaluation and laboratory analysis performed at baseline and at 28 days for assessing the safety and impact on inflammatory markers, which included complete blood counts, C-Reactive protein (CRP), and liver function (alkaline phosphatase, aspartate transaminase, and alanine transaminase). At baseline, there were no statistically significant differences in low back pain when assessed by Roland-Morris function or Oswestry assessments nor were there differences in the blood indices of inflammation. At day 28, both the medical food group and combined therapy group (medical food with naproxen) were statistically significantly superior to the naproxen-alone group (P < 0.05). The medical food and naproxen group showed functional improvement when compared to the naproxen-alone group. The naproxen-alone group showed significant elevations in CRP, alanine transaminase, and aspartate transaminase when compared with the other groups. Medical food alone or with naproxen showed no significant change in liver function tests or CRP, with medical food potentially mitigating the effects seen with naproxen alone. The medical food (Theramine) appeared to be effective in relieving back pain without causing any significant side effects and may provide a safe alternative to presently available therapies.
机译:为了研究新型药物(Theramine)在治疗下背痛中的安全性和有效性,我们对129例患者进行了为期28天的双盲随机对照试验。背痛存在至少6周,且不轻微。患者被随机分配为单独接受医疗食物(n = 43),单独接受萘普生(250 mg / d,n = 42),或同时接受医疗食物和萘普生(n = 44)。所有患者均通过Roland-Morris残疾问卷,Oswestry下背疼痛量表,视觉模拟量表评估以及在基线和第28天进行的实验室分析进行评估,以评估安全性和对炎症标志物的影响,包括全血细胞计数,反应蛋白(CRP)和肝功能(碱性磷酸酶,天冬氨酸转氨酶和丙氨酸转氨酶)。基线时,通过Roland-Morris功能或Oswestry评估,腰背痛没有统计学上的显着差异,炎症血液指标也没有差异。在第28天,医疗食品组和联合治疗组(含萘普生的医疗食品)在统计学上均显着优于单独使用萘普生的组(P <0.05)。与仅使用萘普生的组相比,医用食品和萘普生组显示出功能改善。与其他组相比,仅使用萘普生的组显示出CRP,丙氨酸转氨酶和天冬氨酸转氨酶的显着升高。单独或与萘普生一起使用的医疗食品在肝功能测试或CRP中没有显示出明显的变化,而药用食品可能会减轻单独使用萘普生所产生的影响。医用食品(Theramine)似乎可以有效缓解背部疼痛,而不会引起任何明显的副作用,并且可以为目前可用的疗法提供安全的替代方法。

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