Efficacy of naftopidil in patients with overactive bladder associated with benign prostatic hyperplasia : prospective randomized controlled study to compare differences in efficacy between morning and evening medication
A total of 100 patients with benign prostatic hyperplasia (BPH) and overactive bladder (OAB) symptoms (BPH/OAB), enrolled between June 2006 to March 2008, were randomly divided into 2 groups of morning medication (M) and evening medication (E) groups, then 50 mg of naftopidil was given once a day af...
Veröffentlicht in: | Hinyokika kiyo. Acta urologica Japonica. - 1962. - 57(2011), 1 vom: 08. Jan., Seite 7-13 |
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1. Verfasser: | |
Weitere Verfasser: | , , , , , , , , , , , , , , , |
Format: | Aufsatz |
Sprache: | Japanese |
Veröffentlicht: |
2011
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Zugriff auf das übergeordnete Werk: | Hinyokika kiyo. Acta urologica Japonica |
Schlagworte: | Comparative Study English Abstract Journal Article Randomized Controlled Trial Adrenergic alpha-Antagonists Naphthalenes Piperazines naftopidil R9PHW59SFN |
Zusammenfassung: | A total of 100 patients with benign prostatic hyperplasia (BPH) and overactive bladder (OAB) symptoms (BPH/OAB), enrolled between June 2006 to March 2008, were randomly divided into 2 groups of morning medication (M) and evening medication (E) groups, then 50 mg of naftopidil was given once a day after breakfast or supper for 8 weeks. Data were available for efficacy analysis on 80 patients (M group ; 43, E group ; 37). Naftopidil significantly improved the overall international prostatic symptom score ; from 19.2±7.9 to 11.7±5.8 in the M group and from 19.4±6.4 to 12.3±6.8 in the E group (p<0.0001), QOL score from 4.9±0.8 to 3.2±1.4 in the M group and from 5.0±0.8 to 3.6±1.3 in the E group (p<0.0001), and OAB symptom score from 7.8±2.6 to 5.0±2.5 in the M group (p<0.0001) and from 8.6±2.9 to 5.8± 3.3 in the E group (p<0.0001). There was no significant difference in the incidence of adverse effects between the M group (6.1%) and E group (2.2%). These results suggest that naftopidil improves storage symptoms as well as voiding symptoms regardless of timing of administration |
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Beschreibung: | Date Completed 26.04.2011 Date Revised 15.11.2012 published: Print Citation Status MEDLINE |
ISSN: | 0018-1994 |