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首页> 外文期刊>Open access Journal of Clinical Trials >Phenyramidol in acute conditions of lumbago, integumental pain and musculo-skeletal pain: an open label, noncomparative, multi-center study
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Phenyramidol in acute conditions of lumbago, integumental pain and musculo-skeletal pain: an open label, noncomparative, multi-center study

机译:急性腰痛,皮间痛和肌肉骨骼痛的苯乙酰胺:开放性,非对照,多中心研究

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Objective: To assess the safety and efficacy of phenyramidol hydrochloride tablets in acute conditions of lumbago, integumental pain and musculo-skeletal pain.Methods: This open label, noncomparative, phase IV study recruited adult patients with acute lumbago, integumental pain and musculoskeletal pain who gave written informed consent. Those with elevated liver enzymes, or on analgesics, muscle relaxants, tranquilizers, anti-coagulants, or anti-epileptics were excluded as were pregnant/lactating women. 1 to 2 tablets of 400 mg phenyramidol were given orally 2 to 3 times daily for 3 to 7 days. Safety measures included complete blood count (CBC); liver and renal function tests; electrocardiogram (ECG); global assessments and adverse events. Efficacy measures included change in numerical pain rating scale (NPRS) score and global assessments.Results: 100 patients completed the study. There were no serious adverse events (SAEs) or deaths. The mean (SEM) reduction in the total white blood cell count [0.27 (0.13) thou/μL, P < 0.05] and the mean (SEM) increase in the serum glutamic pyruvic transaminase (SGPT) level [8.78 (3.40) U/L, P < 0.05] were not clinically significant at the end of the treatment period. Investigators’ assessment of safety was: 80% – excellent, 13% – good, 7% – fair. Tolerability grading by patients was: 53% – excellent, 34% – good, 12% – fair; 1% – poor. Out of the total 12 adverse events (AEs) recorded in 11% patients, 7 were clinical, while 5 were laboratory-related pertaining to increased liver enzymes (5%). The average NPRS score showed an improvement of 68% (P < 0.0001). Investigators assessed 89% patients to have clinically meaningful improvement, patients’ assessment of efficacy was: excellent – 43%; good – 38%; fair – 15%; poor – 4%.Conclusion: Phenyramidol is effective and well-tolerated in acute lumbago, musculoskeletal pain and integumental pain when given for up to 7 days. However it should be used with caution in patients with liver disease and with drugs known to cause liver damage.
机译:目的:评估盐酸苯乙拉明片在急性腰痛,皮下痛和肌肉骨骼疼痛中的安全性和有效性。方法:这项开放标签,非对比,IV期研究招募了成年急性腰痛,皮下痛和肌肉骨骼痛的患者。给予书面知情同意。那些肝酶高或使用止痛药,肌肉松弛剂,镇静剂,抗凝剂或抗癫痫药的患者被排除在外,孕妇/哺乳期妇女则被排除在外。每天口服2到3次,每次1至2片400 mg苯乙酰胺,持续3至7天。安全措施包括全血细胞计数(CBC);肝肾功能检查;心电图(ECG);全球评估和不良事件。疗效指标包括数字疼痛评分量表(NPRS)得分的变化和整体评估。结果:100名患者完成了研究。没有严重的不良事件(SAE)或死亡。总白细胞计数的平均值(SEM)降低[0.27(0.13)thou /μL,P <0.05]和血清谷氨酸丙酮酸转氨酶(SGPT)水平的平均值(SEM)升高[8.78(3.40)U / L,P <0.05]在治疗期结束时无临床意义。调查人员对安全性的评估为:80%(优秀),13%(良好),7%(公平)。患者的耐受性等级为:53%–优秀,34%–良好,12%–中等; 1%–较差。在11%的患者中记录的12种不良事件(AE)中,有7例是临床的,而5例与实验室相关的肝酶升高(5%)。 NPRS平均得分提高了68%(P <0.0001)。研究者评估了89%的患者具有临床意义的改善,患者对疗效的评估为:优秀– 43%;好– 38%;公平– 15%;较差– 4%。结论:服用7天后,苯乙酰胺能有效治疗急性腰痛,肌肉骨骼疼痛和皮下痛。但是,对于患有肝病和已知会引起肝损害的药物,应谨慎使用。

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