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Low-dose diclofenac potassium in the treatment of episodic tension-type headache.

机译:小剂量双氯芬酸钾治疗发作性紧张型头痛。

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BACKGROUND: Several clinical trials have demonstrated that low doses of non-steroidal anti-inflammatory drugs relieve episodic tension-type headache (ETH). AIMS: The aims of this placebo-controlled study were to determine whether single doses of diclofenac-K 12.5 and 25mg effectively relieve ETH in adults and to compare it to ibuprofen 400mg. METHODS: A single-dose multicentre, randomised, double-blind, double-dummy, clinical trial was conducted at 22 primary care centres in Germany. All subjects had a history of ETH according to the classification of the International Headache Society. Of 684 subjects randomised, 620 used the study drugs for an episode of tension headache occurring within one month after enrolment: diclofenac-K 12.5mg (n=160), diclofenac-K 25mg (n=156), ibuprofen 400mg (n=151) and placebo (n=153). The primary efficacy variable was total pain relief, calculated as the time-weighted sum of the pain relief assessments from baseline to the 3h evaluation time (TOTPAR-3). RESULTS: For TOTPAR-3, all active treatments were superior to placebo; no statistically significant difference between the three active treatments could be detected. A similar pattern was also observed with regard to TOTPAR-6 (6h evaluation time), > or =50%maxTOTPAR at 3 and 6h, weighted pain intensity difference at 3 and 6h (SPID-3; SPID-6), percentage of patients with complete headache relief at 2h, end of study global evaluation and time to rescue medication. The number-needed-to-treat (NNT) at 6h was 4.5 (2.9-9.2) in the ibuprofen 400mg group, 4.0 (2.8-7.3) in the diclofenac-K 12.5mg group and 3.9 (2.7-7.1) in the diclofenac-K 25mg group. These differences were not statistically significant.CONCLUSION: Diclofenac-K, administered as single doses of 12.5 and 25mg effectively relieves ETH and is comparable to ibuprofen 400mg.
机译:背景:多项临床试验表明,低剂量的非甾体类抗炎药可缓解发作性紧张型头痛(ETH)。目的:这项安慰剂对照研究的目的是确定单剂量双氯芬酸钾12.5和25mg是否能有效缓解成人的ETH,并将其与400mg布洛芬进行比较。方法:在德国的22个初级保健中心进行了单剂量,多中心,随机,双盲,双模拟的临床试验。根据国际头痛协会的分类,所有受试者都有ETH史。在684名随机分组的受试者中,有620名在入选后一个月内出现了紧张性头痛发作:双氯芬酸钾12.5mg(n = 160),双氯芬酸钾25mg(n = 156),布洛芬400mg(n = 151) )和安慰剂(n = 153)。主要功效变量是总的疼痛缓解,计算为从基线到3h评估时间的疼痛缓解评估的时间加权总和(TOTPAR-3)。结果:对于TOTPAR-3,所有积极治疗均优于安慰剂。三种主动治疗之间没有统计学上的显着差异。对于TOTPAR-6(6h评估时间),在3h和6h时大于或等于50%maxTOTPAR,3h和6h时的加权疼痛强度差异(SPID-3; SPID-6),患者百分比也观察到类似的模式在2小时后可完全缓解头痛,研究结束时进行总体评估,并及时挽救药物。布洛芬400mg组在6h时需要治疗的数量(NNT)为4.5(2.9-9.2),双氯芬酸-K 12.5mg组为4.0(2.8-7.3),双氯芬酸为3.9(2.7-7.1) -K 25mg组。结论:双氯芬酸-K,以12.5和25mg的单次剂量给药可有效缓解ETH,与布洛芬400mg相当。

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