Pregled bibliografske jedinice broj: 887636
Randomised clinical trial : a comparative dose‐finding study of three arms of dual release mesalazine for maintaining remission in ulcerative colitis
Randomised clinical trial : a comparative dose‐finding study of three arms of dual release mesalazine for maintaining remission in ulcerative colitis // Alimentary pharmacology & therapeutics, 33 (2011), 3; 313-322 doi:10.1111/j.1365-2036.2010.04537.x (međunarodna recenzija, članak, znanstveni)
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Naslov
Randomised clinical trial : a comparative dose‐finding study of three arms of dual release mesalazine for maintaining remission in ulcerative colitis
Autori
Kruis, W. ; Jonaitis, L. ; Pokrotnieks, J. ; Mikhailova, T.L. ; Horynski, M. ; Bátovský, M.. . ; Lozynsky, YS ; Zakharash, Y. ; Rácz, I. ; Kull, K. ; Včev, Aleksandar ; Faszczyk, M. ; Dilger, K. ; Greinwald, R. ; Mueller, R.
Izvornik
Alimentary pharmacology & therapeutics (0269-2813) 33
(2011), 3;
313-322
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Oral mesalazine ; ulcerative colitis ; remission.
Sažetak
Comparative data regarding different regimens of oral mesalazine (mesalamine) for maintaining remission in ulcerative colitis are limited. To evaluate whether 3.0 g mesalazine once-daily (OD) is superior to the standard treatment of 0.5 g mesalazine three times daily (t.d.s.) and to prove the therapeutic equivalence of OD vs. t.d.s. dosing of total 1.5 g mesalazine for remission maintenance in patients with ulcerative colitis. A 1-year, multicentre, double-blind, double-dummy study was undertaken in patients with endoscopically and histologically confirmed ulcerative colitis in remission. Patients were randomised to oral mesalazine 3.0 g OD, 1.5 g OD or 0.5 g t.d.s. The primary efficacy endpoint was the proportion of patients still in clinical remission at the final visit, with clinical relapse being defined as CAI score >4 and an increase of ≥3 from baseline. The primary efficacy endpoint occurred in 162/217 3.0 g OD patients (75%), 129/212 1.5 g OD patients (61%) and 150/218 0.5 g t.d.s. patients (69%) in the intention-to-treat population, and in 152/177 (86%), 121/182 (67%) and 144/185 (78%) in the per protocol population respectively ; 3.0 g OD was superior to both low-dose regimens for the primary endpoint (i.e. P < 0.001, 3.0 g OD vs. 1.5 g OD ; P = 0.024, 3.0 g OD vs. 0.5 g t.d.s. ; superiority test, per protocol population). Safety analysis, including comprehensive renal monitoring, revealed no concern in any treatment group. Mesalazine 3.0 g once daily was the most effective dose for maintenance of remission in ulcerative colitis of the three regimens assessed, with no penalty in terms of safety.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE