研究目的
To retrospectively assess the effectiveness and safety of a nonablative Er:YAG IntimaLase laser procedure for vaginal laxity in patients treated in clinical practice during a 2.5-year period.
研究成果
The results have confirmed that patients suffering from vaginal laxity can be effectively treated using the nonablative Er:YAG IntimaLase procedure without adverse effects. Randomized controlled trials are necessary to confirm these results with the highest level of clinical evidence.
研究不足
The study is a retrospective case series without a control group or a comparator. The small number of patients in subgroups that estimated efficacy in improving vaginal laxity due to cultural reasons.
1:Experimental Design and Method Selection:
The study was a retrospective case series based on a chart review of patients treated with a nonablative Er:YAG laser for vaginal laxity.
2:Sample Selection and Data Sources:
A total of 364 patients suffering from vaginal laxity were treated in the clinic. Effectiveness was assessed using a Patient Satisfaction Questionnaire and independent evaluation of before and after treatment photographs.
3:List of Experimental Equipment and Materials:
Nonablative Er:YAG laser (XS Dynamis, Fotona, Slovenia) was used.
4:Experimental Procedures and Operational Workflow:
Patients received 2-3 IntimaLase sessions with 30 days interval between the sessions.
5:Data Analysis Methods:
Statistical analysis was performed using GraphPad Prism statistical software.
独家科研数据包,助您复现前沿成果,加速创新突破
获取完整内容