1984
DOI: 10.1185/03007998409109555
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A comparative trial of a controlled-release formulation of ketoprofen (‘Oruvail’) and a conventional capsule formulation of ketoprofen (‘Orudis’) in patients with osteoarthritis of the hip

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Cited by 13 publications
(5 citation statements)
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“…Ketoprofen's half-life in blood plasma was found to be between 2 and 3 h (Martindale, 1996). This short half-life, coupled to the low single administration dosage necessary, renders ketoprofen a very good candidate for the formulation of controlled release dosage forms (Caruso et al, 1982;Houghton et al, 1984a,b;Marcolongo et al, 1984;Morley et al, 1984;Giunchedi et al, 1991;Le Liboux et al, 1994;Habib and Meuse, 1995;Khan et al, 1996;Parejo et al, 1998;Vergote et al, 2001;Roda et al, 2002;Palmieri et al, 2002;Vueba et al, 2004). However, the exact nature of the mechanisms underlying drug controlled release processes is still unknown.…”
Section: Introductionmentioning
confidence: 99%
“…Ketoprofen's half-life in blood plasma was found to be between 2 and 3 h (Martindale, 1996). This short half-life, coupled to the low single administration dosage necessary, renders ketoprofen a very good candidate for the formulation of controlled release dosage forms (Caruso et al, 1982;Houghton et al, 1984a,b;Marcolongo et al, 1984;Morley et al, 1984;Giunchedi et al, 1991;Le Liboux et al, 1994;Habib and Meuse, 1995;Khan et al, 1996;Parejo et al, 1998;Vergote et al, 2001;Roda et al, 2002;Palmieri et al, 2002;Vueba et al, 2004). However, the exact nature of the mechanisms underlying drug controlled release processes is still unknown.…”
Section: Introductionmentioning
confidence: 99%
“…Он эффективен более чем у 98% больных, не вызывает тяжелых НР, не влияет на уровень АД и ЧСС. Лучшую переносимость данной формы кетопрофена по сравнению с обычной отмечали и зарубежные авторы при сравнительном исследовании переносимости обеих форм [31]. По мнению врача и больных, препарат удобен для приема, так что комплаентность при назначении КТД весьма высока (около 98%), а основной причиной пропуска приема препарата было отсутствие боли.…”
Section: заключениеunclassified
“…Minor haematological and biochemical changes during treatment were noted but these were not of clinical importance. Six patients, 2 receiving the controlled-release and 4 receiving the ordinary formulation of ketoprofen, were withdrawn because of lack of efficacy or unacceptable side-effects (120). A multi-centre, double-blind, crossover study was carried out in 80 patients with rheumatoid arthritis to compare the efficacy and side-effect profiles of two formulations of indomethacin.…”
Section: Sustained and Controlled Release Formulationsmentioning
confidence: 99%