Management of Device Detected AT and Impact of Device Treatment Algorithms on Atrial Fibrillation
| 対象疾患 | Cardiovascular Diseases |
|---|---|
| 相 | 該当なし |
| スポンサー | Medtronic Cardiac Rhythm and Heart Failure |
| ステータス | 早期終了 |
| 参加者数 | 79 名 |
| 介入(薬剤) | Treatment arm |
| 開始日 | 2019年10月1日 |
| 完了日 | 2021年7月15日 |
| 結果公開日 | 2026年2月27日 |
概要
The MANDATE-AF study was designed to address evidence needs in India for device-based management of AF using AT/AF (Atrial Tachycardia/Atrial fibrillation) diagnostic features and therapies such as Reactive Atrial anti tachycardia Pacing (rATP) within Medtronic Cardiac Implantable Electronic Devices (CIED)and its impact on the time to persistent AF and progression of AT/AF.
Incidence of 'Persistent AF' Over Time
| Control Arm | 0 percentage probability |
|---|---|
| Treatment Arm | 0 percentage probability |
| Control Arm | 0 percentage probability |
| Treatment Arm | 0 percentage probability |
| Control Arm | 0 percentage probability |
| Treatment Arm | 6.7 percentage probability |
BENITIONS で見る ClinicalTrials.gov の原文を見る
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