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  • HP:0100309: Subdural hemorrhage
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    HP:0100309: Subdural hemorrhage

    Developed by Shray Alag, The Harker School
    Sections: Correlations, Clinical Trials, and HPO

    Correlations computed by analyzing all clinical trials.

    Navigate: Clinical Trials and HPO


    Correlated Drug Terms (4)


    Name (Synonyms) Correlation
    drug3529 Treatment Wiki 1.00
    drug2214 No Treatment Wiki 1.00
    drug3304 Surgical Management + Treatment Wiki 1.00
    Name (Synonyms) Correlation
    drug3303 Surgical Management Wiki 1.00

    Correlated MeSH Terms (3)


    Name (Synonyms) Correlation
    D020200 Hematoma, Subdural, Chronic NIH 1.00
    D006408 Hematoma, Subdural NIH 1.00
    D006406 Hematoma, NIH 1.00

    Correlated HPO Terms (0)


    Name (Synonyms) Correlation

    Clinical Trials

    Navigate: Correlations   HPO

    There is one clinical trial.


    1 A Study of the Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System In the Treatment of Subacute and Chronic Subdural HEmatoma (EMBOLISE)

    The purpose of this study is to evaluate the safety and efficacy of embolization of the middle meningeal artery (MMA) using the Onyx™ Liquid Embolic System (LES) for treatment of symptomatic subacute or chronic subdural hematoma (SDH)

    NCT04402632
    Conditions
    1. Subdural Hematoma
    Interventions
    1. Procedure: Surgical Management
    2. Device: Surgical Management + Treatment
    3. Other: No Treatment
    4. Device: Treatment
    MeSH:Hematoma, Subdural Hematoma, Subdural, Chronic Hematoma
    HPO:Subdural hemorrhage

    Primary Outcomes

    Measure: Effectiveness: Incidence of hematoma recurrence/progression requiring re-intervention

    Time: 90 days post-procedure

    Secondary Outcomes

    Measure: Non-inferiority assessment of Onyx™ LES embolization treatment compared to standard of care based on change in Modified Rankin Scale Score

    Time: 90 days post-procedure

    Measure: Effectiveness: Incidence of hospital readmissions

    Time: 90 days post-procedure

    Measure: Effectiveness: Change in hematoma volume based on CT/MRI imaging

    Time: 90 days post-procedure

    Measure: Effectiveness: Change in hematoma thickness per CT/MRI imaging

    Time: 90 days post-procedure

    Measure: Effectiveness: Change in midline shift based on CT/MRI imaging

    Time: 90 days post-procedure

    Measure: Safety: Incidence of device-related serious adverse events

    Time: 30 days post-procedure

    Measure: Safety: Incidence of procedure-related serious adverse events

    Time: 30 days post-procedure

    Measure: Safety: Incidence of neurological death

    Time: 90 days and 180 days post-procedure

    Measure: Safety: Incidence of device-related adverse events

    Time: 90 days and 180 days post-procedure

    HPO Nodes


    Protein Mutations 0
    SNP 0

    HPO

    Alphabetical listing of all HPO terms. Navigate: Correlations   Clinical Trials


    HPO Nodes


    Protein Mutations 0
    SNP 0

    Reports

    Data processed on September 26, 2020.

    An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.

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