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Compliance, persistence, and preference outcomes of postmenopausal osteoporotic women receiving a flexible or fixed regimen of daily risedronate: A multicenter, prospective, parallel group study

dc.contributor.authorOral, Aydan
dc.contributor.authorLORENC, Roman
dc.date.accessioned2021-03-05T21:42:26Z
dc.date.available2021-03-05T21:42:26Z
dc.date.issued2015
dc.identifier.citationOral A., LORENC R., "Compliance, persistence, and preference outcomes of postmenopausal osteoporotic women receiving a flexible or fixed regimen of daily risedronate: A multicenter, prospective, parallel group study", ACTA ORTHOPAEDICA ET TRAUMATOLOGICA TURCICA, cilt.49, ss.67-74, 2015
dc.identifier.issn1017-995X
dc.identifier.otherav_da35ba06-57ee-4955-bc39-f41040613360
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/143858
dc.identifier.urihttps://doi.org/10.3944/aott.2015.14.0082
dc.description.abstractObjective: The aim of this study was to examine the level of compliance and persistence in patients with postmenopausal osteoporosis (OP) receiving daily risedronate (5 mg) with either fixed dosing of three different timing regimens (A: before breakfast; B: in-between meals; C: before bedtime) or with flexible dosing and the effect on urinary N-terminal telopeptide of Type 1 collagen (NTX-1).
dc.language.isoeng
dc.subjectORTOPEDİ
dc.subjectOrtopedi ve Travmatoloji
dc.subjectCerrahi Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.titleCompliance, persistence, and preference outcomes of postmenopausal osteoporotic women receiving a flexible or fixed regimen of daily risedronate: A multicenter, prospective, parallel group study
dc.typeMakale
dc.relation.journalACTA ORTHOPAEDICA ET TRAUMATOLOGICA TURCICA
dc.contributor.departmentChildren''s Memorial Health Institute , ,
dc.identifier.volume49
dc.identifier.issue1
dc.identifier.startpage67
dc.identifier.endpage74
dc.contributor.firstauthorID11521


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