Brain Densitometric Assessment With Axial Computerized Tomography After Severe Brain Trauma.
調査の概要
状態
詳細な説明
Quantitative analysis of brain and structures in it, in terms of volume, weight and density, in patients with severe brain trauma, using MALUNA dedicated software to process DICOM images.
- st endpoint: compare these data with those obtained by CT scans analysis of patients that recur to this kind of diagnostic investigation for non-traumatic events and with negative diagnostic related to cerebral pathological implication.
- nd endpoint: relate data obtained with clinical evaluation of the patient (cerebral physiology and outcome)
- rd endpoint: evaluate differences in terms of volume, weight and density of brain and its structures, between patients with diffuse cerebral injury and those with localized lesions.
研究の種類
入学 (予想される)
連絡先と場所
研究場所
-
-
-
Varese、イタリア、21100
- Azienda ospedaliera ospedale Circolo e Fondazione Macchi
-
-
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:
- Male and female, any ethnic group
- Patient with severe brain trauma (GCS < 8)
- Need of mechanical ventilation
- Clinical need of urgent CT study of brain.
- Need of clinical control of CT study of brain within first 72 hours from event
- Informed consent obtained from solicitor, due to the fact that patient is
Exclusion Criteria:
- Age minor than 18 yrs old at hospitalization day
- Cardiac arrest pre-hospital or in-hospital and post-anoxic coma
- Non traumatic coma
- Exaggerated ingestion of depressors of central nervous system
- Documented abuse of narcotic drugs;
- Documented abuse of alcohol
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 |
時間枠 |
|---|---|
|
The evaluation of volumetrical and densitometric data of brain tissue of patients with severe brain trauma
時間枠:Participants will be followed for 8 days
|
Participants will be followed for 8 days
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
The evaluation of consciousness.
時間枠:Participants will be followed for 8 days
|
During the observation are evaluated: • Glasgow Coma Scale (GCS). |
Participants will be followed for 8 days
|
|
The evaluation of clinical conditions.
時間枠:Participants will be followed for 8 days
|
During the observation are evaluated multiparametric arterial and venous gas analysis : partial pressure of oxygen in arterial blood(PaO2); partial pressure of carbon dioxide in the arterial blood (PaCO2); cerebral venous oxygen saturation (SjO2); arterial oxygen saturation (SaO2); measure of the acidity or basicity of an aqueous solution (pH); base excess (B.E.); bicarbonate ion (HCO3-); sodium ion (Na+); potassium ion (K+); glycemia; blood concentration of hemoglobin(Hb); hematocrit (Ht). |
Participants will be followed for 8 days
|
|
The evaluation of brain pressures
時間枠:Participants will be followed for 8 days
|
During the observation are evaluating: • Intracranial Cerebral Pressure (ICP) if monitored and perfusional cerebral pressure(PCP); |
Participants will be followed for 8 days
|
|
The evaluation of cardiac monitoring.
時間枠:Participants will be followed for 8 days
|
During the observation are evaluating: • Mean arterial pressure (MAP), cardiac frequency (FC), body temperature, water balance, diuresis; |
Participants will be followed for 8 days
|
協力者と研究者
捜査官
- 主任研究者:Paolo MD Severgnini, Prof.、Università degli Studi dell'Insubria, Varese, Italia
研究記録日
主要日程の研究
研究開始
一次修了 (予想される)
研究の完了 (予想される)
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 (見積もり)
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
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。