🏥 治験ポータル
← 治験一覧に戻る

テリパラチド投与期間がデノスマブ療法前の骨代謝および骨密度に及ぼす影響の検討

基本情報

NCT ID
NCT03702140
ステータス
不明
試験のフェーズ
第2相
試験タイプ
介入
目標被験者数
90
治験依頼者名
Shinshu University

概要

The aim of this study is to examine the efficacy and adverse events in the following 3 groups in osteoporosis patients: 1. The administration period of teriparatide is less than 6 months and thereafter, denosumab for 24 months. 2. The administration period of teriparatide is from 6 to 12 months and thereafter, denosumab for 24 months. 3. The administration period of teriparatide is more than 12 months and thereafter, denosumab for 24 months.

対象疾患

Osteoporosis

介入

"Teriparatide", "Forteo® or Teribon"(DRUG)

依頼者(Sponsor)

実施施設 (1)

中村脳神経内科クリニック

Matsumoto, Nagano, Japan(RECRUITING)