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0.1%维甲酸微球凝胶用于光损伤面部皮肤:一项安慰剂对照试验。

Tretinoin microsphere gel 0.1% for photodamaged facial skin: a placebo-controlled trial.

作者信息

Weiss Jonathan S, Shavin Joel S, Nighland Marge, Grossman Rachel

机构信息

Gwinnett Clinical Research Center, Inc, 2383 Pate St, Snellville, GA 30078-3233, USA.

出版信息

Cutis. 2006 Dec;78(6):426-32.

Abstract

Tretinoin microsphere gel (TMG) 0. 1% was evaluated as a treatment of photodamaged skin. The study included a 6-month, randomized, double-blinded, placebo-controlled phase and an additional 6-month open-label phase during which all subjects received TMG 0. 1%. Forty-five subjects with moderate to severe photodamaged facial skin applied study gel topically to the face once nightly (22 subjects received TMG 0.1% and 23 subjects received placebo). At 6 months, TMG 0. 1% was found to be superior to placebo in improving overall severity of photodamage (P=.0003) and in the investigator's global assessment of clinical response (P<.0001). Statistically significant improvement relative to placebo was observed in fine wrinkling (P<.0001), mottled hyperpigmentation (P=.0002), yellowing/ sallowness (P<.0001), and lentigines (P=.0054). The improvements observed after 6 months of open-label therapy were consistent with the results observed in TMG 0. 1%-treated subjects during double-blinded treatment. Most signs and symptoms of cutaneous irritation were mild throughout the treatment period. At one month, a higher proportion of subjects in the TMG 0. 1% group relative to the placebo group experienced an increase in severity of cutaneous irritation. After 6 months, the difference between treatment groups was statistically significant only for peeling (P=.001) and dryness (P=.007).

摘要

对0.1%的维甲酸微球凝胶(TMG)治疗光损伤皮肤进行了评估。该研究包括一个为期6个月的随机、双盲、安慰剂对照阶段,以及一个为期6个月的开放标签阶段,在此期间所有受试者均接受0.1%的TMG治疗。45名面部皮肤有中度至重度光损伤的受试者每晚在面部局部涂抹研究凝胶一次(22名受试者接受0.1%的TMG,23名受试者接受安慰剂)。6个月时,发现0.1%的TMG在改善光损伤的总体严重程度方面优于安慰剂(P = 0.0003),在研究者对临床反应的整体评估中也优于安慰剂(P < 0.0001)。在细纹(P < 0.0001)、斑驳性色素沉着(P = 0.0002)、发黄/暗沉(P < 0.0001)和雀斑(P = 0.0054)方面,相对于安慰剂观察到了具有统计学意义的改善。开放标签治疗6个月后观察到的改善与双盲治疗期间0.1%的TMG治疗受试者中观察到的结果一致。在整个治疗期间,皮肤刺激的大多数体征和症状都很轻微。在1个月时,0.1%的TMG组相对于安慰剂组有更高比例的受试者皮肤刺激严重程度增加。6个月后,治疗组之间的差异仅在脱皮(P = 0.001)和干燥(P = 0.007)方面具有统计学意义。

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