首页> 外文期刊>BMC Gastroenterology >Nitroglycerin 0.4% ointment vs placebo in the treatment of pain resulting from chronic anal fissure: a randomized, double-blind, placebo-controlled study
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Nitroglycerin 0.4% ointment vs placebo in the treatment of pain resulting from chronic anal fissure: a randomized, double-blind, placebo-controlled study

机译:与安慰剂相比,硝酸甘油软膏0.4%软膏治疗慢性肛裂引起的疼痛:一项随机,双盲,安慰剂对照研究

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Background Complications of chronic anal fissure (CAF) treatments are prompting interest in lower-risk therapies. This study was conducted to compare nitroglycerin (NTG) 0.4% ointment with placebo for pain associated with CAF. Methods In this randomized, double-blind, placebo-controlled trial, patients with one CAF and moderate-to-severe pain (≥50?mm on a 100?mm visual analog scale [VAS]) received 375?mg NTG 0.4% (1.5?mg active ingredient) or 375?mg placebo ointment applied anally every 12?hours for 21?days. The primary end point was change from baseline VAS score in 24-hour pain averaged over days 14–18. Review of data from patients who withdrew early was blinded to treatment. To control for the confounding effects of analgesics, all patients received 650?mg acetaminophen for headache prophylaxis before each application. Results A total of 247 patients were enrolled (NTG, n?=?123; placebo, n?=?124). The prespecified baseline observation carried forward (BOCF) analysis found no significant difference between groups; however, a last observation carried forward (LOCF) analysis showed a significant advantage for NTG. A post hoc analysis (LOCF/BOCF hybrid) demonstrated a significant adjusted mean difference of ?7.0?mm in favor of NTG 0.4% (95% CI ?13.6, –0.4; P?=?.038). Headache was the most common adverse event in the NTG (69.9%) and placebo (47.6%) groups. Conclusions This was the first placebo-controlled study that also controlled for the confounding effects of analgesics used to treat NTG-induced headache. In patients with moderate-to-severe CAF pain, NTG 0.4% ointment effectively reduced CAF pain compared with placebo. Trial registration ClinicalTrials.gov, NCT00522041
机译:背景技术慢性肛裂(CAF)治疗的并发症正引起人们对低风险疗法的兴趣。进行这项研究的目的是将0.4%的硝酸甘油(NTG)软膏与安慰剂比较与CAF相关的疼痛。方法在这项随机,双盲,安慰剂对照试验中,患有一种CAF且中度至重度疼痛(在100?mm视觉模拟量表[VAS]上≥50?mm)的患者接受375?mg NTG 0.4%( 1.5?mg活性成分)或375?mg安慰剂软膏,每12小时一次,持续21天。主要终点是在14到18天中平均24小时疼痛后基线VAS评分的变化。回顾了早退患者的数据,不愿接受治疗。为了控制镇痛药的混杂作用,所有患者在每次应用前均接受650?mg对乙酰氨基酚预防头痛。结果总共招募了247例患者(NTG,n≥123;安慰剂,n≥124)。预先进行的基线观察结转(BOCF)分析发现两组之间无显着差异;但是,最后观察到的结转(LOCF)分析显示了NTG的明显优势。事后分析(LOCF / BOCF混合)表明,调整后的平均均差为7.0毫米,而NTG为0.4%(95%CI≤13.6,-0.4; P≤0.05.038)。头痛是NTG(69.9%)和安慰剂(47.6%)组中最常见的不良事件。结论这是第一项安慰剂对照研究,该研究还控制了用于治疗NTG引起的头痛的镇痛药的混杂作用。在中度至重度CAF疼痛的患者中,与安慰剂相比,NTG 0.4%软膏可有效减轻CAF疼痛。试验注册ClinicalTrials.gov,NCT00522041

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