← 治験一覧に戻る
XIENCE PRIME 日本における市販後調査(PMS)
基本情報
- NCT ID
- NCT01721096
- ステータス
- 完了
- 試験のフェーズ
- -
- 試験タイプ
- 観察
- 目標被験者数
- 536
- 治験依頼者名
- Abbott Medical Devices
概要
The objectives of the PMS are to observe the frequency, type, and degree of device deficiency to assure the safety of the new medical device (XIENCE PRIME) as well as to collect information on evaluation of the efficacy and safety for reevaluation.
対象疾患
AnginaCoronary OcclusionCoronary Artery DiseaseCoronary Artery StenosisMyocardial Ischemia
介入
XIENCE PRIME - Long Length (LL)(DEVICE)
XIENCE PRIME - Core Size(DEVICE)
依頼者(Sponsor)
アボットジャパン(INDUSTRY)
実施施設 (2)
Abbott Vascular Japan Co., Ltd.
Tokyo, Japan
Abbott Vascular Japan Co., Ltd.
Tokyo, Japan