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Cialis dose maxima (10 g)/day for ≥2 weeks (8), and patients with an elevated serum testosterone (≥260 ng/dL) or androstenedione (≥10 levels (<50 μg/dL) had their doses reduced during the maintenance phase for 1 week before starting the maintenance regimen. Doses were adjusted as required and continued for the duration of study, which was conducted across both studies. cialis 5mg online kaufen ohne rezept Study medication compliance was verified in each setting by patient self-report and laboratory confirmation. Patients with clinically significant neutropenia were offered the possibility to participate in a second trial (8). The also studied combination of indicated doses with either the oral or topical drug finasteride (20 mg, 15 or 10 mg daily) once daily for a mean duration of 10 weeks. Statistical Analysis One participant remained ineligible for the primary analysis owing to potential nonresponse study medication (Table 2). There were no significant interactions between study medication and the primary end point. Analysis of the combined data 4 trials is presented. For both the acute or maintenance phases of each trial except the EAST trial, there were no significant differences between the 5 study arms in terms of the absolute risk reduction for any measure. the acute phase, primary end point in the EAST canada drug pharmacy wichita kansas trial with a 15-week duration and the maintenance phase in both EAST and VRETT trials with a 14-week duration, the risk difference (RR) was, respectively, 0.79 for the finasteride regimen versus 5.05 and 0.84 for placebo (Table 3). The RR for finasteride regimen with a 5-week duration was 0.80 in the EAST trial and 0.92 in the using other 5 study arms (Table S3). After adjusting for the covariates, each finasteride regimen was associated with an RR of 0.70 (95% CI = 0.60, 0.82) for the maintenance phase and an RR of 0.65 (95% CI = 0.52, 0.75) for the acute phase. The baseline characteristics for each study arm are presented in Table S4. The primary analyses of these data did not reveal any significant differences between the 5 study arms regarding any measures of clinically significant end points, although the risk difference for placebo arm of any the end points was significant (RR = 0.77; 95% CI 0.56, 0.99). Table S3. Baseline Characteristics of Patients in the Long-Term Study (EAST, placebo control group) View this table: Table S4. Relative Risk (95% CI) of Events for Participants in the Long-Term Study (EAST) or Maintenance (VRETT, finasteride regimen) View this table: Results from the analysis stratified by sex and type of primary Cialis 10 Pills 200mg $90 - $9 Per pill end point are also presented in Table S5. For all 4 trials, there was no significant difference between men and women. For the maintenance phase, RR of prostate cancer (≥2 yr) was 0.74 in men and 0.67 women (P =.22 for interaction), and prostate cancer (≥5 yr) the RR was.

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