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- W2372372681 abstract "Objective To further confirm the Efficacy and safety of tadenan (Pygeum africunum extract) in the treatment of benign prostatic hyperplasia (BPH) in larger population in China. Methods In this open multicenter study,a total of 3 508 patients with symptomatic BPH received oral tadenan of 50 mg twice daily for 8 weeks. Results IPSS,maximum urinary flow and post voiding volume were 19.57± 14.93 ,(13.52±5.36)ml/s and (44.58±30.95)ml four weeks after the treatment of tadenan and were 13.31±11.86,(15.58±5.98)ml/s and (32.64±24.23)ml eight weeks after the treatment,both improved significantly comparing to those before the treatment ( P 0.0001).The volumes of the prostates were reduced.The differences between pre and post treatment were statistically.Adverse events were 1.7% in frequency and generally mild in nature.They could be relieved automatically.No abnormality in routine urine and liver and renal function examinations were found. Conclusions Tadenan offers an alternative for the treatment of patients with BPH.It has satisfactory efficacy and safety profile." @default.
- W2372372681 created "2016-06-24" @default.
- W2372372681 creator A5047488872 @default.
- W2372372681 date "2003-01-01" @default.
- W2372372681 modified "2023-09-25" @default.
- W2372372681 title "Efficacy and safety of a bFGF inhibitor,tadenan in the treatment of benign prostatic hyperplasia:a multicenter trial in China" @default.
- W2372372681 hasPublicationYear "2003" @default.
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