ENT Clinic, University of Vienna, Vienna, Austria.
Clin Drug Investig. 2003;23(9):597-604. doi: 10.2165/00044011-200323090-00006.
To compare the efficacy and safety of ketotifen 0.025% ophthalmic solution (one drop/eye) with placebo as adjunctive therapy to mometasone nasal spray (50 microg/spray, two puffs/nostril) in subjects with seasonal allergic rhinoconjunctivitis (SARC).
Single-centre, randomised, double-masked, two-treatment, two-period crossover study.
8-hour allergen challenge in the Vienna Challenge Chamber.
Subjects were >/=18 years old, had a >/=2-year history of SARC, and were sufficiently responsive to allergen challenge.
During each challenge, subjects received a single dose of mometasone + ketotifen or mometasone + placebo.
47 subjects were randomised, and 44 completed both treatment sequences. Efficacy was based on mean area under the curve (AUC) values for symptom relief scores over time, with the primary variable being the AUC 4-6 hours postdose (AUC(4-6)) for relief of ocular itching. Between-treatment differences were assessed using analysis of variance. While improvement in ocular itching (AUC(4-6)) was observed with both treatments, improvement was significantly (p = 0.014) better with mometasone + ketotifen versus mometasone + placebo, as was improvement based on AUC(0-6) (p = 0.009) and AUC(0-2) (p = 0.006). Similar trends (in favour of mometasone + ketotifen) were observed for improvements in ocular redness, running nose, sneezing and ocular/nasal composite scores (p </= 0.05). None of the safety findings (slit-lamp biomicroscopy, vital signs, adverse events) were clinically significant. One subject discontinued treatment due to mild pharyngitis.
Ketotifen eye drops adjunctive to mometasone nasal spray provided greater relief of both ocular and nasal signs and symptoms than mometasone alone in subjects with SARC.
比较酮替芬 0.025%眼用溶液(1 滴/眼)与安慰剂作为季节性变应性鼻结膜炎(SARC)患者孟鲁司特鼻部喷雾剂(50μg/喷,每侧鼻孔 2 喷)辅助治疗的疗效和安全性。
单中心、随机、双盲、两治疗、两周期交叉研究。
在维也纳挑战室进行 8 小时过敏原挑战。
受试者年龄> = 18 岁,SARC 病史> = 2 年,对过敏原挑战有足够的反应。
在每次挑战中,受试者接受孟鲁司特+酮替芬或孟鲁司特+安慰剂单次剂量。
47 名受试者被随机分组,44 名受试者完成了两种治疗序列。疗效基于症状缓解评分的时间平均曲线下面积(AUC)值,主要变量为 4-6 小时时的 AUC(AUC(4-6))眼部瘙痒缓解。采用方差分析评估治疗间差异。虽然两种治疗均观察到眼部瘙痒(AUC(4-6))改善,但酮替芬+孟鲁司特的改善明显优于孟鲁司特+安慰剂(p = 0.014),AUC(0-6)(p = 0.009)和 AUC(0-2)(p = 0.006)的改善也是如此。对于改善眼部发红、流鼻涕、打喷嚏和眼部/鼻部综合评分(p </= 0.05),也观察到类似的趋势(有利于酮替芬+孟鲁司特)。安全性发现(裂隙灯生物显微镜、生命体征、不良事件)均无临床意义。1 名受试者因轻度咽炎而停止治疗。
酮替芬滴眼剂辅助孟鲁司特鼻部喷雾剂治疗 SARC 患者,在缓解眼部和鼻部症状和体征方面优于孟鲁司特单独治疗。