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临床试验/JPRN-UMIN000020584
JPRN-UMIN000020584已完成未知

Comparative effect of daily teriparatide, weekly teriparatide, or bisphosphonate on bone microarchitecture in patients with primary osteoporosis: A HR-pQCT study - Comparative effect of daily teriparatide, weekly teriparatide, or bisphosphonate in patients with primary osteoporosis

agasaki University Hospital0 个研究点目标入组 130 人开始时间: 2016年1月17日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
130

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
60years-old 至 89years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • 1)Patients with serious cardiac disorder, serious liver dysfunction, serious kidney dysfunction, diabetes mellitus, endocrine and metabolic diseases which may affect to the bone metabolism, and secondary osteoporosis (e.g., glucocorticoid-induced osteoporosis, rheumatoid arthritis, immobilization osteoporosis) 2)Patients treated with medication which affect to the bone metabolism as follows, i)Glucocorticosteroids (within 6 months before enrollment, or >5mg for over 3 months) except inhaler or nasal drip ii)Anti-cancer drugs iii)Anti-osteoporosis drugs (teriparatide, anti-RANKL antibody, bisphosphonates within 6 months before enrollment, SERMs within 3 months before enrollment, or estrogen preparations) 3)Patients who have contraindication of teriparatide or bisphosphonate 4)Patients who have severe allergy 5)Patients enrolled in other clinical studies in the past 3 months. 6)Patients judged to be inadequate for this study by investigators

研究者

发起方
agasaki University Hospital

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