Neodymium Magnet-Guided Removal of Metallic Soft Tissue Foreign Bodies in the Emergency Department
Efficacy and Safety of Neodymium Magnet-Guided Removal of Metallic Foreign Bodies in Soft Tissue in the Emergency Department
The goal of this clinical trial is to learn if a strong magnet (neodymium magnet) can help doctors remove metal objects stuck under the skin in adults. It will also learn about the safety of this method. The main questions it aims to answer are:
- How often can doctors remove the metal object with the help of the magnet?
- How long does the procedure take?
- How often do doctors need to make a cut in the skin, and how long is the cut?
- What problems do participants have within 15 days after the procedure?
- How satisfied are participants with the procedure?
Participants will:
- Have an X-ray to find the metal object
- Have the metal object removed with the help of the magnet in the emergency department, with or without numbing medicine (local anesthetic)
- Come back for a wound check 15 days after the procedure
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
This prospective, single-center, single-arm study is conducted in the Emergency Department of Bursa Uludag University Faculty of Medicine Hospital. Before the procedure, the location of the foreign body and its distance from the skin surface are measured on X-ray, and the entry site is photographed. Before sterile preparation, the magnetic property of the foreign body is confirmed with the neodymium magnet. After sterile preparation, the foreign body is localized with a sterile-draped neodymium magnet. Local anesthesia is applied if needed. The foreign body is removed through the existing wound or, if there is none, through a skin incision. The site is photographed again after removal. Prophylactic antibiotics are given for contaminated wounds. Participants are re-evaluated at suture removal or 15 days after the procedure.
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- 適用できない
連絡先と場所
研究連絡先
研究連絡先
- 名前：Ziya Uzun, MD
- 電話番号：+90 538 737 96 52
- メール：ziyauzun@uludag.edu.tr
研究場所
-
-
Bursa
-
Bursa、Bursa、トルコ（Türkiye）、16059
- 募集
- Bursa Uludag University Faculty of Medicine Hospital, Emergency Department
-
コンタクト：
- Ziya Uzun, MD
- 電話番号：+90 538 737 96 52
- メール：ziyauzun@uludag.edu.tr
-
-
参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Age 18 years or older
- Metallic foreign body in the soft tissue detected on plain radiography
- Foreign body located less than 2 cm from the skin surface
- Foreign body with magnetic properties that interacts with the magnet
- Signed written informed consent
Exclusion Criteria:
- Age under 18 years
- Foreign body located close to structures such as blood vessels, nerves or joint spaces
- Deep location requiring surgical removal
- Inability to cooperate
- Bleeding or coagulation disorder
- Refusal to sign informed consent
研究計画
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：なし
- 介入モデル：単一グループの割り当て
- マスキング：なし（オープンラベル）
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的：Neodymium Magnet-Guided Removal
Adults with a magnetic metallic foreign body in the soft tissue. The foreign body is removed with the help of a neodymium magnet in the emergency department, with or without local anesthesia. |
After sterile preparation, the foreign body is localized and pulled toward the skin surface with a sterile-draped neodymium (NdFeB) magnet, and removed through the existing wound or a skin incision.
他の名前：
|
この研究は何を測定していますか？
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Successful removal of the foreign body
時間枠：During the procedure (Day 0)
|
Number and percentage of foreign bodies successfully removed with the help of the neodymium magnet. |
During the procedure (Day 0)
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Complete removal per participant
時間枠：During the procedure (Day 0)
|
Number and percentage of participants in whom all foreign bodies were successfully removed. |
During the procedure (Day 0)
|
|
Procedure time
時間枠：During the procedure (Day 0)
|
Duration of the foreign body removal procedure, in minutes. |
During the procedure (Day 0)
|
|
Need for additional incision and its length
時間枠：During the procedure (Day 0)
|
Number and percentage of participants who need a new or additional skin incision, and the length of the incision in millimeters, if required. |
During the procedure (Day 0)
|
|
Volume of local anesthetic
時間枠：During the procedure (Day 0)
|
Volume of local anesthetic used during the procedure, in milliliters, in participants who receive local anesthesia. |
During the procedure (Day 0)
|
|
Complications
時間枠：15 days after the procedure
|
Number and percentage of participants with complications (such as wound infection or bleeding) within 15 days after the procedure. |
15 days after the procedure
|
|
Patient satisfaction
時間枠：Immediately after the procedure (Day 0)
|
Participant satisfaction with the procedure on a 5-point Likert scale (1 = not satisfied at all, 5 = very satisfied). Higher scores mean greater satisfaction. |
Immediately after the procedure (Day 0)
|
協力者と研究者
捜査官
捜査官
- 主任研究者：Ziya Uzun, MD、Uludag University
出版物と役立つリンク
一般刊行物
- Shvediuk VV, Elin NE, Dzidzava II, Fufayev EE, Barinov OV. Clinical application of neodymium magnetic instruments for the removal of foreign bodies in blind wounds. Russian Military Medical Academy Reports. 2023;42(2):105-114. doi: 10.17816/rmmar346674.
- Sarihan A, Can C. Soft tissue foreign body removal with magnet in ED settings. Am J Emerg Med. 2014 Aug;32(8):952.e3-5. doi: 10.1016/j.ajem.2014.02.009. Epub 2014 Feb 17. No abstract available.
- Radia R, Suffern R, Pepper T, Fan K. A blacksmith's tale: use of a rare earth magnet to facilitate safe removal of a metallic fragment from the face. Br J Oral Maxillofac Surg. 2020 Dec;58(10):e317-e319. doi: 10.1016/j.bjoms.2020.07.029. Epub 2020 Jul 26.
- Lukish JT, Williams K, Shah A, Mon R, Lukish JR. The Novel Use of Rare Earth Magnets for the Extraction of Metallic Soft Tissue Foreign Bodies in Children. Surg Innov. 2023 Oct;30(5):571-575. doi: 10.1177/15533506231158209. Epub 2023 Mar 14.
研究記録日
主要日程の研究
研究開始 (実際)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
キーワード
その他の研究ID番号
その他の研究ID番号
- 2025-21/14
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?
IPD プランの説明
Individual participant data will not be shared because the informed consent form and ethics approval do not cover sharing of individual-level data with third parties. Aggregated results will be published.
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
米国FDA規制機器製品の研究
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。