Descriptive Study Regarding Ambulant Screening During COVID-19 Pandemia
Descriptive Study Regarding the Ambulant Screening Protocol for COVID-19 in Times of High SARS CoV-2 Prevalence
調査の概要
詳細な説明
The exact prevalence of COVID-19 is unknown. Due to the relatively high number of diagnosed, symptomatic infections despite a strict policy, we expect a high prevalence of COVID 19 throughout the entire population. The risk that an asymptomatic carrier who is admitted to the hospital for a (semi)urgent surgery, treatment of investigation transfers the virus to the hospital staff is very high, and vice versa. This risk is even higher during surgery, where intubation is necessary. Therefore we would like to pre-screen all patients ambulantly on the presence of COVID 19 since there is no consensus for screening at the moment. The golden standard is the SARS CoV-2 PCR on the nasopharyngeal sample together with a CT scan of the lungs. Patients in which a bloodsample is taken as standard of care procedure in this ambulant screening will be asked to give more blood for further investigation.
On top of this standard of care screening, we will perform a questionnaire at the pre-operative visit which evaluates the possible occurence of certain symptoms in the last 2 weeks. These symptoms are fever, anorexia, cough, diarrhea, sneezing, vomiting, dyspnea, headache, rhinorrhea, loss of smell, muscle pain, sputum, sore throat and fatigue. Patients were also asked if one of their housemates are affected by these symptoms. Furthermore, 2 weeks after surgery, patient will be contacted to phone in order to fill the same questionnaire.
研究の種類
入学 (実際)
連絡先と場所
研究場所
-
-
-
Hasselt、ベルギー、3500
- Jessa Hospital
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-
参加基準
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
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- All adult patients > 18 years scheduled for a (semi) urgent surgery, hematological or oncological treatment or elektrophysiciological investigations in the Jessa hospital
Exclusion Criteria:
- Patients < 18 years
- Adult patients who are unable the give informed consent
- Language barrier
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
- 観測モデル:コホート
- 時間の展望:見込みのある
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 |
|---|---|---|
|
Prevalence of symptoms
時間枠:at the ambulant screening
|
Prevalence of fever, cough, anorexia, fatigue, diarrhea, vomiting, dyspnee, sore throat and sputum
|
at the ambulant screening
|
|
Prevalence of positive Sars CoV-2 PCR
時間枠:at the ambulant screening
|
Prevalence of positive COVID 19 tests in patients planned for surgery, treatment or investigation in the hospital
|
at the ambulant screening
|
|
Prevalence of positive radiological findings
時間枠:at the ambulant screening
|
Prevalence of positive radiological findings in CT scans of the lungs of planned for surgery, treatment or investigation in the hospital
|
at the ambulant screening
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Prediction of symptoms
時間枠:2 weeks after surgery or treatment
|
Prediction of symptoms of COVID 19, based on evaluated baseline questionnaire
|
2 weeks after surgery or treatment
|
|
Prediction of symptoms
時間枠:2 weeks after surgery or treatment
|
Prediction of symptoms of COVID 19, based on radiological findings of CT scans
|
2 weeks after surgery or treatment
|
|
Prediction of symptoms
時間枠:2 weeks after surgery or treatment
|
Prediction of symptoms of COVID 19, based on COVID 19 PCR results
|
2 weeks after surgery or treatment
|
協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
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
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- JessaH_COVID19_prescreening
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?
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。