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- W2360635366 abstract "Objective To observe the clinical efficacy of ALA-PDT for treatment of moderate to severe acne vulgaris.Methods Twenty-six cases were assigned to the trail group,and treated by ALA-PDT weekly,twenty minutes for each time;20 cases were assigned to the control group,and treated by blue light weekly,twenty minutes for each time.Meanwhile the control group were treated viaminate capsules 25mg orally and topic clindamycin ointment,twice a day.Course of treatment in both group were 4 weeks.To evaluate the clinical efficacy of pre and post treatment(2nd,4th,6th week).Results On the 4th week,the effective rate(89.47% and 71.43%) of moderate to severe acne vulgaris in the trail group,was higher than that of the control group(60.00% and 0),The difference was statistically significant(all P0.05);On the 6th week,the cure rate(42.31%)and effective rate(92.31%) of trail group was higher than that of control group(cure rate 10.00%,effective rate 55.00%).Conclusion Due to safety,effectiveness and mild adverse reaction,ALA-PDT might become a new method in the treatment of moderate to severe acne vulgaris." @default.
- W2360635366 created "2016-06-24" @default.
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- W2360635366 date "2012-01-01" @default.
- W2360635366 modified "2023-09-23" @default.
- W2360635366 title "Clinical Observation of ALA-PDT for Moderate to Severe Acne Vulgaris" @default.
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