2003
DOI: 10.1136/sti.79.4.270
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Randomised controlled trial and economic evaluation of podophyllotoxin solution, podophyllotoxin cream, and podophyllin in the treatment of genital warts

Abstract: Objectives: To evaluate the efficacy and cost effectiveness of self applied podophyllotoxin 0.5% solution and podophyllotoxin 0.15% cream, compared to clinic applied 25% podophyllin in the treatment of genital warts over 4 weeks. Methods: We conducted a randomised controlled trial in 358 immunocompetent men and women with genital warts of 3 months' duration or less. Results: In the principal analysis both podophyllotoxin solution (OR 2.93, 95% CI 1.56 to 5.50) and podophyllotoxin cream (OR 1.97, 95% CI 1.04 to… Show more

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Cited by 123 publications
(100 citation statements)
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References 18 publications
(16 reference statements)
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“…[60][61][62][63][64][65][66][67][68] No preparation of podophyllotoxin is licensed by the EMA or FDA for the treatment of AGWs, but UK marketing authorisations have been granted for podophyllotoxin 0.5% solution (Condyline ® , Takeda Pharmaceuticals Company Ltd; Warticon ® solution, Stiefel Laboratories Ltd) and 0.15% cream (Warticon ® cream, Stiefel Laboratories Ltd) preparations.…”
Section: Podophyllotoxinmentioning
confidence: 99%
“…[60][61][62][63][64][65][66][67][68] No preparation of podophyllotoxin is licensed by the EMA or FDA for the treatment of AGWs, but UK marketing authorisations have been granted for podophyllotoxin 0.5% solution (Condyline ® , Takeda Pharmaceuticals Company Ltd; Warticon ® solution, Stiefel Laboratories Ltd) and 0.15% cream (Warticon ® cream, Stiefel Laboratories Ltd) preparations.…”
Section: Podophyllotoxinmentioning
confidence: 99%
“…Another compound found in the extract was palmitic acid, which induces mitochondrial pore opening and leads to a decrease of the mitochondrial membrane potential and then to cell death (Belosludtsev et al, 2006). Additionally, podophyllotoxin has been widely used topically in ethanolic solution and creams in the treatment of skin infections (Gilson et al, 2009;Lacey et al, 2003). This may be related to the antileishmanial activity in vivo, as the extract prevents the growth of the lesion without causing irritation or skin damage.…”
Section: Discussionmentioning
confidence: 99%
“…*P < 0.05; **P < 0.01. c The LC3-I and LC3-II proteins were detected by western blotting. The primary epithelial cells were infected with different types Lenti-HPV-E6/E7 virus for 24 h. After 24 h, the infected cells were incubated in culture medium in the presence or absence of the pan-caspase inhibitor Z-VAD-FMK (50 μM) for 30 min and then treated with SR-T100 (5 μg/ml) for 12 h. d The panel shows the percent change in the LC3-II/actin ratio compared with the untreated group in three independent experiments keratinocytes [25]. However, green tea extracts have antitumor and anti-proliferative effects and induce apoptosis in cancer cells by causing G0/G1-phase cell cycle arrest or stabilizing p53 via phosphorylation on critical serine residues [26].…”
Section: Discussionmentioning
confidence: 99%