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首页> 外文期刊>Journal of Indian Society of Periodontology >Comparative evaluation of analgesic and anti-inflammatory efficacy of ibuprofen and traumeel after periodontal flap surgery: A randomized triple-blind clinical trial
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Comparative evaluation of analgesic and anti-inflammatory efficacy of ibuprofen and traumeel after periodontal flap surgery: A randomized triple-blind clinical trial

机译:牙周瓣手术后布洛芬和创伤性镇痛和抗炎效能的比较评价:随机三盲临床试验

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Background: Pain management after performing flap surgery is of paramount importance. Taking into consideration the side effects of nonsteroidal anti-inflammatory drugs (NSAIDs), and the advantages of homeopathic medication, the analgesic and anti-inflammatory properties of ibuprofen (NSAID) and traumeel (homeopathic AID) following flap surgery were evaluated. Materials and Methods: A randomized, triple-blinded, split-mouth clinical trial, with a sample size of 20 (age range of 20–60 years) was planned. Subjects included patients diagnosed with moderate chronic generalized periodontitis. Two quadrants for each subject were operated on, with an interval of 3 weeks. Random assignment of the operated quadrants to the following medication protocols was carried out by a third person: Ibuprofen, 600 mg and traumeel, 600 mg (up to three tablets) every 8 h for first 24 h and SOS (Si Opus Sit/if needed) thereafter for a period of 1 week as pain medication, respectively. After 1 week, sutures were removed. Primary outcomes were mean postoperative pain (modified visual analog scale) and number of tablets consumed in 1 week. The secondary outcome was postoperative tissue response. Any adverse effects were recorded. Results: Number of tablets consumed and pain perception was lower in traumeel compared to ibuprofen Group (P P Conclusion: The present study suggested that while managing pain following flap surgery, traumeel was superior as compared to ibuprofen, with minimal or no side effects.
机译:背景:表演皮瓣外科后的疼痛管理是至关重要的。考虑到非甾体抗炎药(NSAID)的副作用,以及同种疗法用药的优点,评估了瓣手术后布洛芬(NSAID)和创伤(顺势疗法)的镇痛和抗炎特性。材料和方法:计划的随机,三重盲,分裂临床试验,样本量为20(20-60岁)。受试者包括诊断患有中度慢性常规牙周炎的患者。每个受试者的两个象限在开启,间隔为3周。由第三人进行操作象限的随机分配由第三人进行:布洛芬,600毫克和创伤,每8小时600毫克(最多三片),对于前24小时和SOS(SI Opus Sit /如果需要) )此后分别为止痛药的1周。 1周后,缝合被删除。主要结果是平均术后疼痛(修饰的视觉模拟规模)和1周消耗的片剂数量。二次结果是术后组织反应。记录了任何不利影响。结果:与布洛芬组(P P鉴定:目前的研究表明,在瓣膜手术后疼痛的同时,与布洛芬相比,Traumeel的疼痛感染疼痛感知的数量较低,与布洛芬相比,Traumeel具有较小的或无副作用。

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