一种新型家用强脉冲光源用于面部皮肤脱毛的临床评估。
Clinical Evaluation of a Novel Intense Pulsed Light Source for Facial Skin Hair Removal for Home Use.
作者信息
Gold Michael H, Biron Julie A, Thompson Brynne
机构信息
Tennessee Clinical Research Center, Nashville, Tennessee; ; Gold Skin Care Center, Nashville, Tennessee.
Tennessee Clinical Research Center, Nashville, Tennessee;
出版信息
J Clin Aesthet Dermatol. 2015 Jul;8(7):30-5.
OBJECTIVE
The purpose of this Institutional Review Board-approved, open label, prospective study was to study the safety and efficacy of a novel pulsed light home hair removal device in patients with unwanted facial hair.
MATERIALS AND METHODS
Seventeen patients were recruited into the clinical trial; two patients were lost to follow-up. Patients received six biweekly treatments with the novel home-pulsed light device in the facial areas below the level of the cheekbone. Follow-up visits were made at one and three months following the last treatment.
RESULTS
The results showed statistically significant hair reduction numbers (22.7 at baseline to 4.4 at the end of the one-month follow-up time period and 7.0 at the end of the three-month follow-up time period) and percentages of 83.3 percent at one month post home-pulsed light device treatments and 78.1 percent at three months following the novel home-pulsed light device treatments. No adverse events with the device in the clinical evaluation were observed.
CONCLUSION
This novel home use pulsed light device is a safe and effective at-home intense pulsed light device for facial hair removal.
目的
这项经机构审查委员会批准的开放标签前瞻性研究旨在研究一种新型脉冲光家用脱毛设备对面部多余毛发患者的安全性和有效性。
材料与方法
17名患者被纳入临床试验；2名患者失访。患者使用新型家用脉冲光设备在颧骨以下面部区域接受每两周一次的六次治疗。在最后一次治疗后的1个月和3个月进行随访。
结果
结果显示毛发减少数量具有统计学意义（基线时为22.7，在1个月随访期结束时为4.4，在3个月随访期结束时为7.0），在家用脉冲光设备治疗后1个月毛发减少百分比为83.3%，在新型家用脉冲光设备治疗后3个月为78.1%。在临床评估中未观察到该设备的不良事件。
结论
这种新型家用脉冲光设备是一种安全有效的家用强脉冲光面部脱毛设备。
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