A dose-escalation study to assess the efficacy and safety of sildenafil citrate in men with erectile dysfunction

被引:53
作者
Meuleman, E
Cuzin, B
Opsomer, RJ
Hartmann, U
Bailey, MJ
Maytom, MC
Smith, MD
Osterloh, IH
机构
[1] Acad Ziekenhuis, Dept Urol, NL-6500 HB Nijmegen, Netherlands
[2] Hop Edouard Herriot, Serv Urol, Lyon, France
[3] Clin Univ St Luc, Div Urol, B-1200 Brussels, Belgium
[4] Med Hsch Hannover, Arbeitsbereich Klin Psychol, Hannover, Germany
[5] Epsom Gen Hosp, Surrey, England
[6] Pfizer Inc, New York, NY 10016 USA
[7] Pfizer Cent Res, Sandwich, Kent, England
关键词
erectile dysfunction; sildenfil; dose-escalation study; efficacy;
D O I
10.1046/j.1464-410x.2001.00998.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objective To assess the efficacy and safety of sildenafil citrate (Viagra(R), Pfizer Inc., USA) in a double-blind, placebo-controlled, dose-escalation study over a period of 26 weeks in men with erectile dysfunction of a broad spectrum of aetiology. Patients and methods In all, 315 patients from five countries were randomized to receive treatment with placebo (156 men) or sildenafil (159 men). Significant concomitant medical conditions were hypertension (20%), a history of pelvic surgery (19%), diabetes mellitus (15%), and ischaemic heart disease (10%). Patients randomized to treatment received a starting dose of 25 mg of sildenafil or matching placebo, which could be increased to 50 mg and then to 100 mg of sildenafil, based on efficacy and tolerability. Assessments of efficacy comprised the 15-item International Index of Erectile Function (IIEF), including question three (ability to achieve an erection) and question four (ability to maintain an erection), a partner questionnaire, an overall efficacy question, and event-log data. Results After 12 weeks of treatment, 26%, 32% and 42% of patients were taking 25, 50 and 100 mg of sildenafil, respectively. A similar distribution of doses was reported after 26 weeks of treatment. Treatment with sildenafil significantly improved the patients' abilities to achieve and maintain an erection compared with treatment with placebo (P < 0.001). Scores for four of the five sexual function domains of the IIEF (erectile function, orgasmic function, intercourse satisfaction and overall satisfaction) also improved significantly (P < 0.001). There was a significant improvement in the mean score for the erectile function domain. regardless of the aetiology of erectile dysfunction (P < 0.001). After 12 weeks and 26 weeks of treatment, 82% and 79% of patients receiving sildenafil reported improved erections, compared with 24% and 23% of patients receiving placebo, respectively (P < 0.001). Treatment-related adverse events were mild to moderate and occurred in 27% of patients receiving sildenafil, compared with 8% of patients receiving placebo. Conclusion Sildenafil is an effective and well-tolerated treatment for men with erectile dysfunction of a broad spectrum of aetiology.
引用
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页码:75 / 81
页数:7
相关论文
共 24 条
  • [1] SEXUAL FUNCTIONING IN PATIENTS WITH CHRONIC RENAL-FAILURE
    ABRAM, HS
    HESTER, LR
    SHERIDAN, WF
    EPSTEIN, GM
    [J]. JOURNAL OF NERVOUS AND MENTAL DISEASE, 1975, 160 (03) : 220 - 226
  • [2] PHYSIOLOGY OF PENILE ERECTION
    ANDERSSON, KE
    WAGNER, G
    [J]. PHYSIOLOGICAL REVIEWS, 1995, 75 (01) : 191 - 236
  • [3] [Anonymous], 1960, Urological Survey
  • [4] BENET AE, 1995, UROL CLIN N AM, V22, P699
  • [5] Sildenafil, a novel effective oral therapy for male erectile dysfunction
    Boolell, M
    GepiAttee, S
    Gingell, JC
    Allen, MJ
    [J]. BRITISH JOURNAL OF UROLOGY, 1996, 78 (02): : 257 - 261
  • [6] Boolell M, 1996, Int J Impot Res, V8, P47
  • [7] ROLE OF NITRIC BRIDE IN THE PHYSIOLOGY OF ERECTION
    BURNETT, AL
    [J]. BIOLOGY OF REPRODUCTION, 1995, 52 (03) : 485 - 489
  • [8] CHRONIC ADVANCED LIVER-DISEASE AND IMPOTENCE - CAUSE AND EFFECT
    CORNELY, CM
    SCHADE, RR
    VANTHIEL, DH
    GAVALER, JS
    [J]. HEPATOLOGY, 1984, 4 (06) : 1227 - 1230
  • [9] Dinsmore WW, 1998, BRIT J UROL, V81, P437
  • [10] DROLLER MJ, 1993, JAMA-J AM MED ASSOC, V270, P83