• Je něco špatně v tomto záznamu ?

Cizolirtine citrate is safe and effective for treating urinary incontinence secondary to overactive bladder: a phase 2 proof-of-concept study

F. Zát'ura, J. Všetiča, M. Abadías, I. Pavlík, P. Schraml, M. Brod'ák, J. Villoria, M. Sust

. 2010 ; 57 (1) : 145-152.

Jazyk angličtina Země Švýcarsko

Typ dokumentu klinické zkoušky, fáze II, srovnávací studie, časopisecké články, multicentrická studie, randomizované kontrolované studie, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc12025573

BACKGROUND: Antimuscarinic agents currently dominate medical treatment for urinary incontinence secondary to overactive bladder (OAB). Alternatives to improve their risk-benefit ratio are welcomed. OBJECTIVE: To demonstrate the efficacy and safety of oral cizolirtine citrate in this indication. DESIGN, SETTING, AND PARTICIPANTS: A randomised, double-blind, placebo- and active-controlled, phase 2 multicentre clinical trial performed by urologists or gynaecologists at referral centres. A sample was composed of 135 outpatients with signs of lower urinary tract dysfunction and urodynamically documented detrusor overactivity; 20 patients left the study prematurely, chiefly (n=10) because of adverse events. INTERVENTION: Allocation to treatments was asymmetrical (2:2:1) to cizolirtine citrate 800 mg/d, placebo, or oxybutynin 15 mg/d. Treatments were given for 12 wk. MEASUREMENTS: Efficacy measures included a bladder diary, filling- and voiding-phase urodynamic evaluations, and measure of quality of life (QoL). Adverse events were systematically recorded. Statistical procedures included analysis of covariance, chi(2) tests, and calculation of 95% confidence intervals. RESULTS AND LIMITATIONS: Most patients (92.6%) were female, and their mean age was 51.8 yr. Bladder diary variables improved significantly with active drug over placebo: The average number of voidings per 24 h was reduced by 33.4%, 17.0%, and 34.3% (p=0.001) in the cizolirtine citrate, placebo, and oxybutynin groups, respectively. The mean estimated voided volume per voluntary micturition increased by 17.8%, 0%, and 14.5% (p=0.002) in the cizolirtine citrate, placebo, and oxybutynin groups, respectively. The proportions of patients achieving fewer than eight voidings per 24 h, complete dryness, or both were also superior with active drugs over placebo. Only cizolirtine showed significant superiority over placebo to improve urodynamic parameters, although the asymmetrical allocation played against oxybutynin in the inferences. Cizolirtine citrate caused fewer antimuscarinic but more gastrointestinal (nausea) and neurologic (headache and vertigo) adverse events than oxybutynin. CONCLUSIONS: Cizolirtine citrate is a promising agent in the treatment of OAB with urinary incontinence.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc12025573
003      
CZ-PrNML
005      
20221005174457.0
007      
ta
008      
120816s2010 sz f 000 0#eng||
009      
AR
024    7_
$a 10.1016/j.eururo.2009.04.045 $2 doi
035    __
$a (PubMed)19446951
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a sz
100    1_
$a Záťura, František, $d 1951- $7 jo2002107483 $u Department of Urology, Olomouc University Hospital, Olomouc, Czech Republic.
245    10
$a Cizolirtine citrate is safe and effective for treating urinary incontinence secondary to overactive bladder: a phase 2 proof-of-concept study / $c F. Zát'ura, J. Všetiča, M. Abadías, I. Pavlík, P. Schraml, M. Brod'ák, J. Villoria, M. Sust
520    9_
$a BACKGROUND: Antimuscarinic agents currently dominate medical treatment for urinary incontinence secondary to overactive bladder (OAB). Alternatives to improve their risk-benefit ratio are welcomed. OBJECTIVE: To demonstrate the efficacy and safety of oral cizolirtine citrate in this indication. DESIGN, SETTING, AND PARTICIPANTS: A randomised, double-blind, placebo- and active-controlled, phase 2 multicentre clinical trial performed by urologists or gynaecologists at referral centres. A sample was composed of 135 outpatients with signs of lower urinary tract dysfunction and urodynamically documented detrusor overactivity; 20 patients left the study prematurely, chiefly (n=10) because of adverse events. INTERVENTION: Allocation to treatments was asymmetrical (2:2:1) to cizolirtine citrate 800 mg/d, placebo, or oxybutynin 15 mg/d. Treatments were given for 12 wk. MEASUREMENTS: Efficacy measures included a bladder diary, filling- and voiding-phase urodynamic evaluations, and measure of quality of life (QoL). Adverse events were systematically recorded. Statistical procedures included analysis of covariance, chi(2) tests, and calculation of 95% confidence intervals. RESULTS AND LIMITATIONS: Most patients (92.6%) were female, and their mean age was 51.8 yr. Bladder diary variables improved significantly with active drug over placebo: The average number of voidings per 24 h was reduced by 33.4%, 17.0%, and 34.3% (p=0.001) in the cizolirtine citrate, placebo, and oxybutynin groups, respectively. The mean estimated voided volume per voluntary micturition increased by 17.8%, 0%, and 14.5% (p=0.002) in the cizolirtine citrate, placebo, and oxybutynin groups, respectively. The proportions of patients achieving fewer than eight voidings per 24 h, complete dryness, or both were also superior with active drugs over placebo. Only cizolirtine showed significant superiority over placebo to improve urodynamic parameters, although the asymmetrical allocation played against oxybutynin in the inferences. Cizolirtine citrate caused fewer antimuscarinic but more gastrointestinal (nausea) and neurologic (headache and vertigo) adverse events than oxybutynin. CONCLUSIONS: Cizolirtine citrate is a promising agent in the treatment of OAB with urinary incontinence.
650    _2
$a dospělí $7 D000328
650    _2
$a rozdělení chí kvadrát $7 D016009
650    _2
$a interval spolehlivosti $7 D016001
650    _2
$a dvojitá slepá metoda $7 D004311
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a lidé $7 D006801
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a kyseliny mandlové $x škodlivé účinky $x terapeutické užití $7 D008333
650    _2
$a lidé středního věku $7 D008875
650    _2
$a antagonisté muskarinových receptorů $x škodlivé účinky $x terapeutické užití $7 D018727
650    _2
$a pyrazoly $x škodlivé účinky $x terapeutické užití $7 D011720
650    _2
$a kvalita života $7 D011788
650    _2
$a časové faktory $7 D013997
650    _2
$a výsledek terapie $7 D016896
650    _2
$a hyperaktivní močový měchýř $x komplikace $x farmakoterapie $x patofyziologie $7 D053201
650    _2
$a inkontinence moči $x farmakoterapie $x etiologie $x patofyziologie $7 D014549
650    _2
$a urodynamika $x účinky léků $7 D014563
651    _2
$a Česká republika $7 D018153
651    _2
$a Španělsko $7 D013030
655    _2
$a klinické zkoušky, fáze II $7 D017427
655    _2
$a srovnávací studie $7 D003160
655    _2
$a časopisecké články $7 D016428
655    _2
$a multicentrická studie $7 D016448
655    _2
$a randomizované kontrolované studie $7 D016449
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Všetička, Jaroslav $7 xx0139549
700    1_
$a Abadías, Montserrat $7 gn_A_00000141
700    1_
$a Pavlík, Ivan, $d 1958- $7 xx0084177
700    1_
$a Schraml, Peter $u Department of Urology, Masarykova Hospital, Usti nad Labem, Czech Republic
700    1_
$a Broďák, Miloš, $d 1968- $7 xx0079082
700    1_
$a Villoria, Jesús
700    1_
$a Sust, Mariá
773    0_
$w MED00001669 $t European urology $x 1873-7560 $g Roč. 57, č. 1 (2010), s. 145-152
910    __
$a ABA008 $b sig $c sign $y m $z 0
990    __
$a 20120816 $b ABA008
991    __
$a 20221005174453 $b ABA008
999    __
$a ok $b bmc $g 947615 $s 782919
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2010 $b 57 $c 1 $d 145-152 $i 1873-7560 $m European urology $n Eur Urol $x MED00001669
LZP    __
$a Pubmed-20120816/10/02

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...