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心不全の証拠がある成人の治療における不足を対象とした必要な鉄の注入 (INITIATE-HF)

2026年9月28日 更新者:Alan Go、Kaiser Permanente

心不全の証拠で治療されている成人における不足鉄の目標注入

The INITIATE-HF study is a cluster randomized controlled trial that aims to find out if reminding doctors about treatment guidelines for iron deficiency in adults with heart failure who are hospitalized and have evidence of iron deficiency changes the subsequent use of intravenous (IV) iron.

Two groups of hospitalized adult patients with known heart failure and iron deficiency will be compared:

  • Group 1 will include doctors who receive a notification with their patient's iron storage test results and guideline recommendations related to the use of IV iron.
  • Group 2 will include doctors who do not receive this notification and continue with usual standard of care.

The study will measure if this provider-facing notification affects physician use of recommended IV iron treatment in eligible patients with heart failure, left ventricular ejection fraction less than 50%, and iron deficiency. Secondarily, if there is an increased use of IV iron observed in the intervention group, this study will evaluate whether there are differential health outcomes (i.e., fewer subsequent hospital visits and lower risk of death) of patients whose providers were assigned to the intervention group.

調査の概要

詳細な説明

The INITIATE-HF study will be managed at the Kaiser Permanente Northern California (KPNC) Division of Research and will include participants from KPNC medical centers. Up to 21 medical centers will be randomly assigned into two groups, with balanced populations between the groups based on demographic and heart failure-related characteristics. In medical centers assigned to the intervention group, physicians of eligible patients with heart failure and iron deficiency (i.e., TSAT <20%) will be sent information from current KPNC and national clinical practice guidelines about the use of IV iron therapy in the setting of heart failure. In medical centers assigned to the control group, physicians will not be contacted about their patients with iron deficiency or receive information about current guidelines about the use of IV iron (i.e., usual care). If a patient with heart failure is admitted to a medical center assigned to the intervention group and has iron deficiency, their treating doctor will be notified about their patient's iron stores lab results, information from KPNC and national guidelines about the use of IV iron therapy, and details about the available IV iron formulations and recommended dosages for their consideration. The study team will not have any direct contact with patients at any of the medical centers assigned to either the intervention or control group and will not be involved in any clinical care decision-making for any patients, as that will reside with each patient's responsible physician and care team.

The intention-to-treat (ITT) population will consist of patients meeting all eligibility criteria at both intervention and control sites. The per-protocol population will include data from all patients at intervention sites. All primary and secondary endpoints will be analyzed using mixed effects Cox proportional hazards regression for point and interval estimation of the intervention effect on the primary outcome and on each of the secondary outcomes. Similarly, mixed effects Poisson regression will be additionally performed to analyze the effect of the intervention in relation to secondary outcomes when characterized as counts: all-cause and heart failure-specific outpatient encounters (i.e., clinic and telehealth visits), emergency department visits, and hospitalizations.

Interaction analyses will be performed to assess for potential heterogeneity of treatment effects based on the following prespecified subgroups: age, sex, race/ethnicity, presumed etiology of heart failure (i.e., ischemic vs. non-ischemic), duration of diagnosed heart failure (i.e., <1 vs. >1 year), reason for hospital admission (i.e., primary vs. secondary discharge diagnosis for heart failure), left ventricular ejection fraction category (<40% vs. 41-49%), B-type natriuretic peptide (BNP) level (i.e., < vs. > the median value), TSAT (i.e., <15% vs. 15-19%), estimated glomerular filtration rate (eGFR) level (i.e., < vs. > the median), hemoglobin level (i.e., < vs. > the median), anemia status, and KPNC service area.

The primary analysis will focus on the implementation outcome of the administration of IV iron during the index hospitalization to determine how the provider-facing notification influences provider behavior and care processes. The secondary analysis will evaluate effectiveness outcomes, including the composite of all-cause death and heart failure-related hospitalization, to determine whether any observed changes in the implementation process outcome also translate into improved patient clinical outcomes up through 12 months after randomization.

研究の種類

介入

入学 (推定)

400

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Alan S Go, MD
  • 電話番号:510-821-0904
  • メール:alan.s.go@kp.org

研究場所

    • California
      • Pleasanton、California、アメリカ、94588
        • 募集
        • Division of Research
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

Adults (age >18 years); Diagnosed heart failure with most recent left ventricular ejection fraction <50%; Hospitalized for any reason for the index admission; Documented iron deficiency defined as TSAT <20% during the index hospitalization; At least 6 months of health plan coverage and prescription drug benefit before admission

Exclusion Criteria:

A documented allergy to IV iron in the Kaiser Permanente Northern California (KPNC) electronic health record (EHR) system; A history of hemochromatosis (i.e., iron overload) based on KPNC EHR data; End-stage kidney disease (defined as receiving chronic dialysis or a prior kidney transplant) or advanced chronic kidney disease (i.e., estimated glomerular filtration rate [eGFR] <30 mL/min/1.73 m2) based on most recent pre-admission outpatient laboratory results or the KPNC regional End-Stage Kidney Disease Treatment Registry; Serum ferritin >300 ng/mL based on KPNC EHR data; Diagnosed with metastatic cancer and/or receiving systemic chemotherapy based on KPNC EHR data; Institutionalized (e.g., prison) and/or receiving palliative care per KPNC EHR data

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:他の
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ:Intervention Medical Center - Notification Group

In medical centers assigned to the intervention group, physicians of eligible patients will be sent a one-time notification with information about their patient's iron deficiency, current KPNC and national clinical practice guidelines about IV iron therapy, and available IV iron formulations and recommended dosages.

In medical centers assigned to the intervention group within the INITIATE-HF study, physicians of eligible patients with HF and iron deficiency will be sent information from current KPNC and national guidelines about IV iron therapy.

アクティブコンパレータ:Control Medical Center - No Notification Group

In medical centers assigned to the control group, physicians of eligible patients will NOT be sent information about their patients or current KPNC and national clinical practice guidelines about the use of IV iron therapy in the setting of heart failure.

In medical centers assigned to the control group, physicians will not receive information about current guidelines about the use of IV iron (i.e., usual care).

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
% of patients receiving IV iron within 7 days of hospital admission
時間枠:From the day of confirmed eligibility up to 7 days later

The primary outcome is the implementation outcome of the percentage of patients who receive IV iron within 7 days of hospitalization to determine how the provider-facing notification influences provider behavior and care processes.

From the day of confirmed eligibility up to 7 days later

二次結果の測定

結果測定
メジャーの説明
時間枠
% of patients who experience the composite outcome of all-cause death and heart failure-related hospitalization
時間枠:From randomization to the end of 12 months after randomization

The secondary outcome will be a percentage of patients who experience the composite outcome of all-cause death and heart failure-related hospitalization, to determine whether any observed changes in the implementation process outcome also translate into improved patient outcomes during the 12 months after randomization.

From randomization to the end of 12 months after randomization

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年4月20日

一次修了 (推定)

2027年12月1日

研究の完了 (推定)

2028年12月31日

試験登録日

最初に提出

2026年2月19日

QC基準を満たした最初の提出物

2026年3月11日

最初の投稿 (実際)

2026年3月12日

学習記録の更新

投稿された最後の更新 (実際)

2026年10月1日

QC基準を満たした最後の更新が送信されました

2026年9月28日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

De-identified individual participant data underlying the results of this trial will be considered for sharing with qualified researchers. Requests must include a scientifically sound proposal and documentation of IRB approval or exemption. Data access will be subject to review and execution of an appropriate data use agreement to protect participant privacy.

IPD 共有時間枠

Requests for IPD will be considered starting 6 months after publication of the primary results of the study, with an end date of 10 years after study closure. Supporting information will be available as of 09 MAR 2026, with no end date.

IPD 共有アクセス基準

De-identified individual participant data underlying the results of this trial will be considered for sharing with qualified researchers. Requests must include a scientifically sound proposal and documentation of IRB approval or exemption. Data access will be subject to review and execution of an appropriate data use agreement to protect participant privacy.

There will be no restriction to access supporting information.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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