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橈骨遠位端骨折後の即時動員と 2 週間のギプス固定の比較 (LIMPER-DRF)

2026年10月31日 更新者:Aleksi Reito、Tampere University Hospital

即時の動員と 2 週間のギプス固定 - 前向き、無作為化、対照試験の研究プロトコル

The aim of this study is to analyze total lenght of the sick leace and functional outcome (PRWE) at 2 months between 2 weeks casting and immediate mobilization following volar plating for a DRF.

調査の概要

詳細な説明

This study is a prospective, randomized, controlled trial. The aim of this study will be to compare the early postoperative outcomes of the patients enrolled in the early mobilization with those patients in post-operative 2-week casting following volar plating for a DRF. Co-primary outcome in this study will be the total lenght of sick leave and Patient-Rated Wrist Evaluation (PRWE) 2 months after the operation.

研究の種類

介入

入学 (推定)

240

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。

研究場所

      • Danderyd、スウェーデン
        • Danderyds Sjukhus
      • Sundsvall、スウェーデン
        • Sundsvalls sjukhuset
      • Jyväskylä、フィンランド
        • Teemu Karjalainen
      • Kuopio、フィンランド
        • Kuopio University Hospital
      • Tampere、フィンランド
        • Laura Kärnä

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~65年 (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:

  • Intra- or extra articular DRF (Colles, Smith, Volar barton)
  • operative treatment justified

Exclusion Criteria:

  • Refusal to participate in the study
  • Open fracture with a severity greater than Gustilo grade 1
  • Patient aged less than 18 or over 65
  • Patient does not understand written or spoken guidance in local languages
  • Pathological fracture
  • Previous fracture in the same wrist or forearm in the last 10 years, that has led to impairment of function
  • Ipsilateral fracture in upper extremity
  • Associated fractures of the ulna (except fractures of the PSU)
  • Polytrauma

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:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:橈骨遠位端骨折後、掌側ロッキングプレートで治療した場合の即時動員

Immediate mobilization postoperatively without casting

Volar plating of distal radius fracture

アクティブコンパレータ:橈骨遠位端骨折後の 2 週間のギプス固定は掌側ロッキング プレートで治療

Volar plating of distal radius fracture

Dorsal cast placed in OR

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
Patient-rated wrist evaluation questionnaire
時間枠:2 months

The PRWE is a 15-item questionnaire designed to measure wrist pain and disability in daily activities. It ranges from 100 (worst) to 0 (best). It consists of 2 subscales. Pain subscale contains 5 items. Function subscale contains total 10 items which are further divided into 2 sections: specific activities (having 6 items) and usual activities.

2 months
Total lenght of the sick leave
時間枠:12 months

Total number of days of work during the 1 year study period

12 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Patient-rated wrist evaluation questionnaire
時間枠:4 weeks

The PRWE is a 15-item questionnaire designed to measure wrist pain and disability in daily activities. It ranges from 100 (worst) to 0 (best). It consists of 2 subscales. Pain subscale contains 5 items. Function subscale contains total 10 items which are further divided into 2 sections: specific activities (having 6 items) and usual activities.

4 weeks
Patient-rated wrist evaluation questionnaire
時間枠:6 months

The PRWE is a 15-item questionnaire designed to measure wrist pain and disability in daily activities. It ranges from 100 (worst) to 0 (best). It consists of 2 subscales. Pain subscale contains 5 items. Function subscale contains total 10 items which are further divided into 2 sections: specific activities (having 6 items) and usual activities.

6 months
Patient-rated wrist evaluation questionnaire
時間枠:12 months

The PRWE is a 15-item questionnaire designed to measure wrist pain and disability in daily activities. It ranges from 100 (worst) to 0 (best). It consists of 2 subscales. Pain subscale contains 5 items. Function subscale contains total 10 items which are further divided into 2 sections: specific activities (having 6 items) and usual activities.

12 months
Return to work
時間枠:4 weeks

Patient is asked if he or she has returned to the previous work. If no patient is asked is he or she Still on sick leave, partial sick leave or returned to other work.

4 weeks
Return to work
時間枠:2 months

Patient is asked if he or she has returned to the previous work. If no patient is asked is he or she Still on sick leave, partial sick leave or returned to other work.

2 months
Return to work
時間枠:6 months

Patient is asked if he or she has returned to the previous work. If no patient is asked is he or she Still on sick leave, partial sick leave or returned to other work.

6 months
Return to work
時間枠:12 months

Patient is asked if he or she has returned to the previous work. If no patient is asked is he or she Still on sick leave, partial sick leave or returned to other work.

12 months
Complications
時間枠:4 weeks

Any surgery related complication: wound dehiscence, deep infection, flexor tendon rupture, nerve injury, mechanical complications, nonunion, malunion, complex regional pain syndrome

4 weeks
Complications
時間枠:2 months

Any surgery related complication: wound dehiscence, deep infection, flexor tendon rupture, nerve injury, mechanical complications, nonunion, malunion, complex regional pain syndrome

2 months
Complications
時間枠:6 months

Any surgery related complication: wound dehiscence, deep infection, flexor tendon rupture, nerve injury, mechanical complications, nonunion, malunion, complex regional pain syndrome

6 months
Complications
時間枠:12 months

Any surgery related complication: wound dehiscence, deep infection, flexor tendon rupture, nerve injury, mechanical complications, nonunion, malunion, complex regional pain syndrome

12 months
Self-perceived working ability
時間枠:4 weeks

Patient is asked to rate his os her working ability using two scales: NRS from 0 (fully disabled) to 10 (best capability) and ordinally (fully capable, partially capable, fully disabled).

4 weeks
Self-perceived working ability
時間枠:2 months

Patient is asked to rate his os her working ability using two scales: NRS from 0 (fully disabled) to 10 (best capability) and ordinally (fully capable, partially capable, fully disabled).

2 months
Self-perceived working ability
時間枠:6 months

Patient is asked to rate his os her working ability using two scales: NRS from 0 (fully disabled) to 10 (best capability) and ordinally (fully capable, partially capable, fully disabled).

6 months
Self-perceived working ability
時間枠:12 months

Patient is asked to rate his os her working ability using two scales: NRS from 0 (fully disabled) to 10 (best capability) and ordinally (fully capable, partially capable, fully disabled).

12 months
Visual analogue pain scale
時間枠:4 weeks

Overall pain during last 7 days in a scale from 0 to 100 (worst)

4 weeks
Visual analogue pain scale
時間枠:2 months

Overall pain during last 7 days in a scale from 0 to 100 (worst)

2 months
Visual analogue pain scale
時間枠:6 months

Overall pain during last 7 days in a scale from 0 to 100 (worst)

6 months
Visual analogue pain scale
時間枠:12 months

Overall pain during last 7 days in a scale from 0 to 100 (worst)

12 months
Patient-acceptable symptom state
時間枠:2 months

Patient satisfaction will be measured using the patient-acceptable symptom state (PASS).The questionnaires will include the following questions: Would you be willing to take the same treatment again if the treatment result was as it is now? (Yes/No) Considering all the different ways your injury is affecting you, if you would remain in this state, do you feel that your current state is satisfactory (Yes/No)?

2 months
Patient-acceptable symptom state
時間枠:6 months

Patient satisfaction will be measured using the patient-acceptable symptom state (PASS).The questionnaires will include the following questions: Would you be willing to take the same treatment again if the treatment result was as it is now? (Yes/No) Considering all the different ways your injury is affecting you, if you would remain in this state, do you feel that your current state is satisfactory (Yes/No)?

6 months
Patient-acceptable symptom state
時間枠:12 months

Patient satisfaction will be measured using the patient-acceptable symptom state (PASS).The questionnaires will include the following questions: Would you be willing to take the same treatment again if the treatment result was as it is now? (Yes/No) Considering all the different ways your injury is affecting you, if you would remain in this state, do you feel that your current state is satisfactory (Yes/No)?

12 months
Work capacity
時間枠:4 weeks

The participants will be asked to rate their working capacity on a numerical scale from 0 to 10, with "0" being not able to work at all and "10" being the ability to work at its best.

4 weeks
Work capacity
時間枠:2 months

The participants will be asked to rate their working capacity on a numerical scale from 0 to 10, with "0" being not able to work at all and "10" being the ability to work at its best.

2 months
Work capacity
時間枠:6 months

The participants will be asked to rate their working capacity on a numerical scale from 0 to 10, with "0" being not able to work at all and "10" being the ability to work at its best.

6 months
Work capacity
時間枠:12 months

The participants will be asked to rate their working capacity on a numerical scale from 0 to 10, with "0" being not able to work at all and "10" being the ability to work at its best.

12 months

その他の成果指標

結果測定
メジャーの説明
時間枠
Patient activity
時間枠:4 weeks

Patient activity measured with triaxial wrist accelerometer

4 weeks

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

捜査官

  • スタディディレクター:Aleksi Reito、Tampere University Hospital
  • 主任研究者:Laura Kärnä, MD、Tampere University Hospital

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

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)

2021年12月1日

一次修了 (実際)

2026年2月10日

研究の完了 (推定)

2027年2月10日

試験登録日

最初に提出

2021年10月7日

QC基準を満たした最初の提出物

2021年11月26日

最初の投稿 (実際)

2021年12月9日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月4日

QC基準を満たした最後の更新が送信されました

2026年10月31日

最終確認日

2026年10月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • R21111

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

Data is available on reasonable request.

IPD 共有時間枠

After the study has been completed and for 10 years after.

IPD 共有アクセス基準

On reasonable request and research plan for IPD use should be provided.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE

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米国FDA規制医薬品の研究

いいえ

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いいえ

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