Abstract | INTRODUCTION: We performed a prospective, randomized study to examine the efficacies of levofloxacin and doxazosin alone and as a combination therapy in patients with National Institutes of Health (NIH) category III chronic prostatitis/chronic pelvic pain syndrome. PATIENTS AND METHODS: Men with a NIH diagnosis of category III chronic prostatitis/chronic pelvic pain syndrome and who had experienced pelvic pain for more than 3 months during the last 6 months were enrolled. All patients underwent treatment for 6 weeks. The patients were assessed at baseline and after 2 and 6 weeks by using the NIH Chronic Prostatitis Symptom Index. Eighty-one men (average age 40.1 years) were randomized to either the levofloxacin group (n = 26), the doxazosin group (n = 26), or the combination group (n = 29). RESULTS: The average baseline NIH Chronic Prostatitis Symptom Index total scores were 22.6, 22.4, and 24.1, respectively. At 6 weeks, the total scores were 11.2 (response rate 50.3%), 17.7 (response rate 21.1%), and 13.1 (response rate 45.6%), respectively. The levofloxacin group showed a higher response rate than the doxazosin group, not at 2 weeks but at 6 weeks (p < 0.001). CONCLUSIONS:
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Authors | Chang Wook Jeong, Dae Jung Lim, Hwancheol Son, Sang Eun Lee, Hyeon Jeong |
Journal | Urologia internationalis
(Urol Int)
Vol. 80
Issue 2
Pg. 157-61
( 2008)
ISSN: 1423-0399 [Electronic] Switzerland |
PMID | 18362485
(Publication Type: Journal Article, Randomized Controlled Trial)
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Chemical References |
- Adrenergic alpha-Antagonists
- Anti-Bacterial Agents
- Levofloxacin
- Ofloxacin
- Doxazosin
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Topics |
- Adrenergic alpha-Antagonists
(therapeutic use)
- Adult
- Anti-Bacterial Agents
(therapeutic use)
- Doxazosin
(therapeutic use)
- Drug Therapy, Combination
- Humans
- Levofloxacin
- Male
- Middle Aged
- Ofloxacin
(therapeutic use)
- Prospective Studies
- Prostatitis
(drug therapy)
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