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Effect of adjunctive diclofenac with verteporfin therapy to treat choroidal neovascularization due to age-related macular degeneration: phase II study.

机译:附有维替泊芬治疗的双氯芬酸辅助治疗老年性黄斑变性引起的脉络膜新生血管形成的效果:II期研究。

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BACKGROUND: To determine short-term effects of topical diclofenac administered in conjunction with verteporfin therapy for predominantly classic subfoveal choroidal neovascularization (CNV) due to age-related macular degeneration (AMD). METHODS: Randomized, multicenter (14), prospective, placebo-controlled, double-masked clinical trial. Patients (n=61) were randomly assigned to treatment with diclofenac sodium ophthalmic solution 0.1% or placebo and followed for 12 weeks. Patients instilled diclofenac or placebo two drops four times daily, 2-4 days before verteporfin treatment until 2 weeks after treatment, then two drops twice daily for 10 weeks. This exploratory study was not powered to detect differences between treatment groups. Statistical analyses were conducted solely to aid interpretation of results. RESULTS: In diclofenac-treated eyes, mean changes in visual acuity letter score from baseline in the diclofenac and placebo groups were +1.8 letters and -1.0 at week 1 (P=0.505 between groups). Mean visual acuity letter scores decreased in both groups at all subsequent visits, with a mean change at 12 weeks of -7.4 with diclofenac and -2.6 with placebo (P=0.213). Percentages of eyes with stable or improved vision (change or=5 letters) were similar in the diclofenac and placebo groups at all study visits. No significant between-group differences in changes from baseline in lesion area, greatest linear dimension (GLD), fluorescein leakage, or retinal thickness were detected. CONCLUSION: In patients with predominantly classic subfoveal CNV due to AMD, administration of topical diclofenac with verteporfin therapy was associated with similar vision outcomes to placebo plus verteporfin therapy.
机译:背景:确定局部使用双氯芬酸与韦替泊芬治疗联合使用对因年龄相关性黄斑变性(AMD)引起的主要典型的小凹下脉络膜新生血管(CNV)的近期效果。方法:随机,多中心(14),前瞻性,安慰剂对照,双掩蔽临床试验。患者(n = 61)被随机分配接受0.1%双氯芬酸钠眼药水或安慰剂治疗,并随访12周。患者在维替泊芬治疗前2-4天每天两次滴注双氯芬酸或安慰剂,直到治疗后2周,然后每天两次滴注两次,共10周。这项探索性研究无力检测治疗组之间的差异。仅进行统计分析以帮助解释结果。结果:在双氯芬酸治疗的眼睛中,双氯芬酸和安慰剂组的视力字母得分相对于基线的平均变化在第1周时为+1.8个字母和-1.0(各组之间P = 0.505)。在随后的所有随访中,两组的平均视力字母得分均下降,双氯芬酸在12周时的平均变化为-7.4,而安慰剂组为-2.6(P = 0.213)。在所有研究访问中,双氯芬酸和安慰剂组中视力稳定或改善(改变≤4或增加≥5的眼睛)的眼睛百分比相似。在病变区域,最大线性尺寸(GLD),荧光素渗漏或视网膜厚度方面,未发现基线之间的组间差异。结论:在因AMD导致主要为典型的中心凹下CNV的患者中,局部给予双氯芬酸和维替泊芬治疗与安慰剂加维替泊芬治疗具有相似的视觉效果。

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