BENITIONSClinical Trial Intelligence

Fluid Management of Acute Decompensated Heart Failure Subjects Treated With Reprieve Decongestion Management System (DMS)

該当なし 完了 NCT05174312

対象疾患Acute Decompensated Heart Failure
該当なし
スポンサーReprieve Cardiovascular, Inc
ステータス完了
参加者数100 名
介入(薬剤)Reprieve Decongestion Management System, Diuretic
開始日2022年7月11日
完了日2025年1月10日
結果公開日2026年5月29日

概要

The objective of this study is to prospectively compare decongestive therapy administered by the Reprieve DMS system to Optimal Diuretic Therapy (ODT) in the treatment of patients diagnosed with acute decompensated heart failure (ADHF). The main objective is to determine if the Reprieve DMS can more efficiently decongest ADHF patients in comparison to Control Therapy.

Total Urine Sodium Output

24 hours post-treatment initiation · mmol of sodium

Reprieve Decongestion Management System1082 ± 487 mmol of sodium
Optimal Diuretic Therapy423 ± 290 mmol of sodium
p-value<0.001

Clinically Significant Acute Kidney Injury, Severe Electrolyte Abnormality, Symptomatic Hypotension or Hypertensive Emergency.

End of treatment, 0-72 hours. · total number of events

Reprieve Decongestion Management System16 total number of events
Optimal Diuretic Therapy19 total number of events
p-value0.43

BENITIONS で見る ClinicalTrials.gov の原文を見る

同じ疾患の他の治験

すべての治験

このページは ClinicalTrials.gov の公開データをまとめたものです。医学的助言ではなく、投資助言でもありません。必ず専門医にご相談ください。