| 試験進捗状況 | 開始前/Preinitiation |
| UMIN試験ID | UMIN000044379 |
| 受付番号 | R000050695 |
| 科学的試験名 | 脆弱性大腿骨近位部骨折患者における骨格筋量の横断的調査 |
| 一般公開日(本登録希望日) | 2021/10/01 |
| 最終更新日 | 2021/06/02 (2版) |
| 基本情報/Basic information | |||
| 一般向け試験名/Public title | 脆弱性大腿骨近位部骨折患者における骨格筋量の横断的調査 | A cross-sectional study of skeletal muscle mass in patients with fragility proximal femoral fractures. | |
| 一般向け試験名略称/Acronym | MuMaFra | MuMaFra | |
| 科学的試験名/Scientific Title | 脆弱性大腿骨近位部骨折患者における骨格筋量の横断的調査 | A cross-sectional study of skeletal muscle mass in patients with fragility proximal femoral fractures. | |
| 科学的試験名略称/Scientific Title:Acronym | MuMaFra | MuMaFra | |
| 試験実施地域/Region |
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| 対象疾患/Condition | |||
| 対象疾患名/Condition | 脆弱性大腿骨近位部骨折 | fragility proximal femoral fractures | |
| 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 | 骨粗鬆症を基盤とする脆弱性骨折のうち、大腿骨近位部骨折は寝たきりの原因として挙げられるため、手術を含めた早期からの治療介入が重要である。治療成績には様々な要因が提起されているが、骨格筋量の関与についての報告はまれであるため、本研究により明らかにする。 | Among fragility fractures based on osteoporosis, proximal femoral fracture is one of the most common causes of bedridden patients, so early intervention including surgery is important. Although various factors have been proposed to affect the outcome of treatment, the involvement of skeletal muscle mass has rarely been reported, and this study will clarify this issue. |
| 目的2/Basic objectives2 | その他/Others | |
| 目的2 -その他詳細/Basic objectives -Others | 骨粗鬆症を基盤とする大腿骨近位部骨折治療のため当院に入院した患者に対し、入院中の適切な時期(概ね術後2週以内)に、通常診療のための検査に加えて骨密度測定を行う。この時健側の大腿骨近位部と全身のDual-energy X-ray Absorptiometry(DXA)を測定し、受傷時の骨格筋量と術後運動機能回復度の関連を調査する。 | Patients admitted to our hospital for treatment of osteoporosis-based proximal femoral fractures will undergo bone mineral density measurement at an appropriate time during hospitalization (generally within 2 weeks after surgery) in addition to the usual medical examination. Dual-energy X-ray absorptiometry of the healthy side of proximal femur and the whole body will be measured to investigate the relationship between skeletal muscle mass at the time of injury and the degree of recovery of postoperative motor function. |
| 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 | 脆弱性大腿骨近位部骨折患者の受傷時の骨格筋量と術後運動機能回復度の関連 | Relationship between skeletal muscle mass at the time of injury and the degree of postoperative motor function recovery in patients with fragility proximal femoral fractures |
| 副次アウトカム評価項目/Key secondary outcomes | 1.脆弱性大腿骨近位部骨折患者の受傷時におけるサルコペニア有病率
2.脆弱性大腿骨近位部骨折患者の受傷時骨格筋量と骨密度との関連 3.脆弱性大腿骨近位部骨折患者の受傷時骨格筋量と骨折型との関連 4.脆弱性大腿骨近位部骨折患者の受傷時骨格筋量と骨代謝マーカーとの関連 5.脆弱性大腿骨近位部骨折患者の受傷時骨格筋量と受傷前の運動機能との関連 6.脆弱性大腿骨近位部骨折患者の受傷時骨格筋量と術後成績との関連 |
1.Prevalence of sarcopenia at the time of injury in patients with fragility fracture of the proximal femur
2. Relationship between skeletal muscle mass and bone mineral density at the time of injury in patients with fragility proximal femoral fractures 3. Relationship between skeletal muscle mass at injury and fracture type in patients with fragility proximal femoral fracture. 4. Relationship between skeletal muscle mass at injury and bone metabolic markers in patients with fragility proximal femoral fracture. 5. Relationship between skeletal muscle mass at injury and pre-injury motor function in patients with fragility proximal femoral fracture. 6. Relationship between skeletal muscle mass at injury and postoperative outcomes in patients with fragility proximal femoral fractures. Translated with www.DeepL.com/Translator (free version) |
| 基本事項/Base | ||
| 試験の種類/Study type | 観察/Observational | |
| 試験デザイン/Study design | ||
| 基本デザイン/Basic design | ||
| ランダム化/Randomization | ||
| ランダム化の単位/Randomization unit | ||
| ブラインド化/Blinding | ||
| コントロール/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 | ||
| 介入の目的/Purpose of intervention | ||
| 介入の種類/Type of intervention | ||
| 介入1/Interventions/Control_1 | ||
| 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 | ・倫理委員会承認後~2024年12月31日の期間
・済生会中津病院整形外科において ・脆弱性大腿骨近位部骨折により入院加療した患者 |
_Between the approval date of the Ethics Committee and December 31, 2024
_Patients admitted to the Department of Orthopaedic Surgery at Saiseikai Nakatsu Hospital with fragility of proximal femoral fracture |
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| 除外基準/Key exclusion criteria | ・必要な検査が施行できない患者
・その他、担当医が不適当と判断した患者 |
_Patients for whom necessary tests cannot be performed
_Other patients deemed inappropriate by the physician in charge |
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| 目標参加者数/Target sample size | 300 | ||||
| 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 | 大阪府済生会中津病院 | Osaka Saiseikai Nakatsu Hospital | ||||||||||||
| 所属部署/Division name | 整形外科 | Department of Orthopaedic Surgery | ||||||||||||
| 郵便番号/Zip code | 530-0012 | |||||||||||||
| 住所/Address | 大阪市北区芝田2-10-39 | 2-10-39 Shibata, kita-Ku, Osaka CIty | ||||||||||||
| 電話/TEL | 06-6372-0333 | |||||||||||||
| Email/Email | k_inui2@nakatsu.saiseikai.or.jp | |||||||||||||
| 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 | 大阪府済生会中津病院 | Osaka Saiseikai Nakatsu Hospital | ||||||||||||
| 部署名/Division name | 整形外科 | Department of Orthopaedic Surgery | ||||||||||||
| 郵便番号/Zip code | 530-0012 | |||||||||||||
| 住所/Address | 大阪市北区芝田2-10-39 | 2-10-39 Shibata, kita-Ku, Osaka CIty | ||||||||||||
| 電話/TEL | 06-6372-0333 | |||||||||||||
| 試験のホームページURL/Homepage URL | ||||||||||||||
| Email/Email | k_inui2@nakatsu.saiseikai.or.jp | |||||||||||||
| 実施責任組織/Sponsor | ||
| 機関名/Institute | その他 | Osaka Saiseikai Nakatsu Hospital |
| 機関名/Institute (機関選択不可の場合) |
大阪府済生会中津病院 | |
| 部署名/Department | 整形外科 | |
| 研究費提供組織/Funding Source | ||
| 機関名/Organization | その他 | Osaka Saiseikai Nakatsu Hospital |
| 機関名/Organization (機関選択不可の場合) |
大阪府済生会中津病院 | |
| 組織名/Division | 整形外科 | |
| 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 | 大阪府済生会中津病院倫理委員会 | Ethics Committee of Osaka Saiseikai Nakatsu Hospital |
| 住所/Address | 大阪市北区芝田2-10-39 | 2-10-39 Shibata, kita-Ku, Osaka CIty |
| 電話/Tel | 06-6372-0333 | |
| Email/Email | k_inui2@nakatsu.saiseikai.or.jp | |
| 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 | ||
| 主な結果/Results | ||
| 主な結果入力日/Results date posted | ||
| 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 | 開始前/Preinitiation | |||||||
| 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 | ||||||||
| 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 | ①患者基本情報:年齢、性別、診断名、身長、体重、併存症・既往歴(循環器疾患、代謝性疾患、脳卒中、骨粗鬆症、鬱、認知症)、骨粗鬆症治療歴、受傷前後ADL
②血液検査結果:CBC, AST, ALT, 血清Cre, eGFR, CRP, LDH, ALP, CK, TP, Alb, 25OH-VitD、骨代謝マーカー ③X線検査:大腿骨近位部骨折評価・術後評価のための画像 ④CT画像:大腿骨近位部骨折評価・術後評価のための画像 ⑤Dual-energy X-ray Absorptiometry:全身モードと大腿骨近位部 ⑥大腿骨近位部骨折関連:受傷から手術までの期間、骨折型、 ⑦手術関連:手術時間、出血量、手術方法、術中特記事項 |
1) Basic patient information: age, sex, diagnosis, body mass index, complications and past history (circulatory disease, metabolic disease, stroke, osteoporosis, depression, cognitive disorder), osteoporosis treatment, ADL before and after injury
2) Blood test: CBC, AST, ALT, serum Cre, eGFR, CRP, LDH, ALP, CK, TP, Alb, 25OH-VitD, bone metabolic marker 3) X-ray examination 4) CT image 5) Dual-energy X-ray Absorptiometry: Whole Body Model and Proximalfemur 6) Information on fracture: period from injury to surgery, fracture type (7) Surgery: operation time, blood loss, operation method, and intraoperative special notes |
| 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://upload.umin.ac.jp/cgi-open-bin/ctr/ctr_view.cgi?recptno=R000050695 |
| URL(英語) | https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000050695 |