| 試験進捗状況 | 試験終了/Completed |
| UMIN試験ID | UMIN000046998 |
| 受付番号 | R000053608 |
| 科学的試験名 | 代謝性アシドーシスと貧血との関連 |
| 一般公開日(本登録希望日) | 2022/02/24 |
| 最終更新日 | 2022/02/24 (1版) |
| 基本情報/Basic information | |||
| 一般向け試験名/Public title | 血液透析患者における代謝性アシドーシスと貧血
との関連 |
Relationship between metabolic acidosis and anemia
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| 一般向け試験名略称/Acronym | 代謝性アシドーシスと貧血との関連 | Relationship between metabolic acidosis and anemia | |
| 科学的試験名/Scientific Title | 代謝性アシドーシスと貧血との関連 | Relationship between metabolic acidosis and anemia | |
| 科学的試験名略称/Scientific Title:Acronym | 代謝性アシドーシスと貧血との関連 | Relationship between metabolic acidosis and anemia | |
| 試験実施地域/Region |
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| 対象疾患/Condition | |||
| 対象疾患名/Condition | 血液透析患者 | hemodialysis | |
| 疾患区分1/Classification by specialty |
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| 疾患区分2/Classification by malignancy | 悪性腫瘍以外/Others | ||
| ゲノム情報の取扱い/Genomic information | いいえ/NO | ||
| 目的/Objectives | ||
| 目的1/Narrative objectives1 | アルカリ化剤の重曹錠を内服させ貧血との関連
を検討する。 |
Oral sodium bicarbonate tablets and association with anemia To consider. |
| 目的2/Basic objectives2 | 有効性/Efficacy | |
| 目的2 -その他詳細/Basic objectives -Others | ||
| 試験の性質1/Trial characteristics_1 | ||
| 試験の性質2/Trial characteristics_2 | ||
| 試験のフェーズ/Developmental phase | ||
| 評価/Assessment | ||
| 主要アウトカム評価項目/Primary outcomes | Hbが上昇したかどうか | Whether Hb is increaseed or not |
| 副次アウトカム評価項目/Key secondary outcomes | ||
| 基本事項/Base | ||
| 試験の種類/Study type | 介入/Interventional | |
| 試験デザイン/Study design | ||
| 基本デザイン/Basic design | 単群/Single arm | |
| ランダム化/Randomization | 非ランダム化/Non-randomized | |
| ランダム化の単位/Randomization unit | ||
| ブラインド化/Blinding | オープン/Open -no one is blinded | |
| コントロール/Control | 群内/Self control | |
| 層別化/Stratification | ||
| 動的割付/Dynamic allocation | ||
| 試験実施施設の考慮/Institution consideration | ||
| ブロック化/Blocking | ||
| 割付コードを知る方法/Concealment | ||
| 介入/Intervention | |||
| 群数/No. of arms | 1 | ||
| 介入の目的/Purpose of intervention | 予防・検診・検査/Prevention | ||
| 介入の種類/Type of intervention |
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| 介入1/Interventions/Control_1 | アルカリ化剤の重曹錠を内服させ貧血との関連
を検討した。 |
Alkalizing agent sodium bicarbonate tablets were administered internally, and the relationship with anemia was examined.
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| 介入2/Interventions/Control_2 | |||
| 介入3/Interventions/Control_3 | |||
| 介入4/Interventions/Control_4 | |||
| 介入5/Interventions/Control_5 | |||
| 介入6/Interventions/Control_6 | |||
| 介入7/Interventions/Control_7 | |||
| 介入8/Interventions/Control_8 | |||
| 介入9/Interventions/Control_9 | |||
| 介入10/Interventions/Control_10 | |||
| 適格性/Eligibility | |||||
| 年齢(下限)/Age-lower limit |
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| 年齢(上限)/Age-upper limit |
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| 性別/Gender | 男女両方/Male and Female | ||||
| 選択基準/Key inclusion criteria | Hbの変動が±0.5g/dl以下と少ない患者 | Patients with less than 0.5 g/dl variation in Hb levels. | |||
| 除外基準/Key exclusion criteria | Hbの変動が±0.6g/dl以上と多い患者 | Patients with high Hb levels variability of more than 0.6 g/dl. | |||
| 目標参加者数/Target sample size | 16 | ||||
| 責任研究者/Research contact person | ||||||||||||||
| 責任研究者/Name of lead principal investigator |
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| 所属組織/Organization | だいもん内科・腎透析クリニック | Department of Nephrology, Daimon Clinic for Internal Medicine, Nephrology and Dialysis | ||||||||||||
| 所属部署/Division name | 臨床工学科 | Clinical Engineering | ||||||||||||
| 郵便番号/Zip code | 9218802 | |||||||||||||
| 住所/Address | 石川県野々市市押野1-400 | 1-400 oshino nonoichi ishikawa Japan | ||||||||||||
| 電話/TEL | 076-294-0066 | |||||||||||||
| Email/Email | sdbjr617@gmail.com | |||||||||||||
| 試験問い合わせ窓口/Public contact | ||||||||||||||
| 試験問い合わせ窓口担当者/Name of contact person |
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| 組織名/Organization | だいもん内科・腎透析クリニック | Department of Nephrology, Daimon Clinic for Internal Medicine, Nephrology and Dialysis | ||||||||||||
| 部署名/Division name | 臨床工学科 | Clinical Engineering | ||||||||||||
| 郵便番号/Zip code | 9218802 | |||||||||||||
| 住所/Address | 石川県野々市市押野1-400 | 1-400 oshino nonoichi ishikawa Japan | ||||||||||||
| 電話/TEL | 0762940066 | |||||||||||||
| 試験のホームページURL/Homepage URL | ||||||||||||||
| Email/Email | sdbjr617@gmail.com | |||||||||||||
| 実施責任組織/Sponsor | ||
| 機関名/Institute | その他 | Department of Nephrology, Daimon Clinic for Internal Medicine, Nephrology and Dialysis |
| 機関名/Institute (機関選択不可の場合) |
だいもん内科・腎透析クリニック | |
| 部署名/Department | ||
| 研究費提供組織/Funding Source | ||
| 機関名/Organization | 無し | none |
| 機関名/Organization (機関選択不可の場合) |
無し | |
| 組織名/Division | ||
| 組織の区分/Category of Funding Organization | その他/Other | |
| 研究費拠出国/Nationality of Funding Organization | ||
| その他の関連組織/Other related organizations | ||
| 共同実施組織/Co-sponsor | ||
| その他の研究費提供組織/Name of secondary funder(s) | ||
| IRB等連絡先(公開)/IRB Contact (For public release) | ||
| 組織名/Organization | だいもん内科・腎透析クリニック | Department of Nephrology, Daimon Clinic for Internal Medicine, Nephrology and Dialysis |
| 住所/Address | 石川県野々市市押野1-400 | 1-400 oshino nonoichi ishikawa Japan |
| 電話/Tel | 0762940066 | |
| Email/Email | sdbjr617@gmail.com | |
| 他機関から発行された試験ID/Secondary IDs | ||
| 他機関から発行された試験ID/Secondary IDs | いいえ/NO | |
| 試験ID1/Study ID_1 | ||
| ID発行機関1/Org. issuing International ID_1 | ||
| 試験ID2/Study ID_2 | ||
| ID発行機関2/Org. issuing International ID_2 | ||
| 治験届/IND to MHLW | ||
| 試験実施施設/Institutions | ||
| 試験実施施設名称/Institutions | ||
| その他の管理情報/Other administrative information | ||||||||
| 一般公開日(本登録希望日)/Date of disclosure of the study information |
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| 関連情報/Related information | ||
| プロトコル掲載URL/URL releasing protocol | ||
| 試験結果の公開状況/Publication of results | 未公表/Unpublished | |
| 結果/Result | ||||||||
| 結果掲載URL/URL related to results and publications | ||||||||
| 組み入れ参加者数/Number of participants that the trial has enrolled | 16 | |||||||
| 主な結果/Results | pHは炭酸水素ナトリウム投与前が7.3885、5週間後が7.3893、20週間後が7.3834であり、炭酸水素ナトリウムを投与した場合のpHは7.3885であった。一方、HCO3は、炭酸水素ナトリウム投与前22.661、5週間後24.431、20週間後25.563と徐々に増加した(表2)。
Hb値(主要評価項目)はほぼ横ばいであった(図1)。 |
The pH was 7.3885 before, 7.3893 after 5 weeks, and 7.3834 after 20 weeks of treatment with sodium bicarbonate. In contrast, HCO3 increased gradually from 22.661 before, to 24.431 after 5 weeks, and 25.563 after 20 weeks treatment with sodium bicarbonate (Table 2).
The Hb levels (primary endpoint) were almost unchanged (Figure 1). |
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| 主な結果入力日/Results date posted |
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| 結果掲載遅延/Results Delayed | ||||||||
| 結果遅延理由/Results Delay Reason | ||||||||
| 最初の試験結果の出版日/Date of the first journal publication of results | ||||||||
| 参加者背景/Baseline Characteristics | ||||||||
| 参加者の流れ/Participant flow | ||||||||
| 有害事象/Adverse events | ||||||||
| 評価項目/Outcome measures | ||||||||
| 個別症例データ共有計画/Plan to share IPD | ||||||||
| 個別症例データ共有計画の詳細/IPD sharing Plan description | ||||||||
| 試験進捗状況/Progress | ||||||||
| 試験進捗状況/Recruitment status | 試験終了/Completed | |||||||
| プロトコル確定日/Date of protocol fixation |
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| 倫理委員会による承認日/Date of IRB |
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| 登録・組入れ開始(予定)日/Anticipated trial start date |
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| フォロー終了(予定)日/Last follow-up date |
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| 入力終了(予定)日/Date of closure to data entry | ||||||||
| データ固定(予定)日/Date trial data considered complete | ||||||||
| 解析終了(予定)日/Date analysis concluded | ||||||||
| その他/Other | ||
| その他関連情報/Other related information | ||
| 管理情報/Management information | ||||||||
| 登録日時/Registered date |
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| 最終更新日/Last modified on |
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| 閲覧ページへのリンク/Link to view the page | |
| URL(日本語) | https://center6.umin.ac.jp/cgi-open-bin/ctr/ctr_view.cgi?recptno=R000053608 |
| URL(英語) | https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000053608 |