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D002532: Intracranial Aneurysm

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 (2)


Name (Synonyms) Correlation
drug386 BNT162b3 Wiki 1.00
drug3645 WEB embolization Wiki 1.00

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D000783 Aneurysm, NIH 1.00

Correlated HPO Terms (2)


Name (Synonyms) Correlation
HP:0002617 Vascular dilatation HPO 1.00
HP:0004944 Dilatation of the cerebral artery HPO 1.00

Clinical Trials

Navigate: Correlations   HPO

There is one clinical trial.


1 Comparison of Woven EndoBridge Device Sizing With Conventional Measurements and Virtual Simulation Using the Sim&Size Software: A Multi-Center Experience

Selection of the appropriate size of the device is mandatory during aneurysm treatment with a WEB. The Investigators aimed to investigate if virtual simulation with Sim&Size software may have an impact on technical, angiographic, and clinical outcomes after WEB treatment. Data from two large-volume centers were collected and compared (January 2017-January 2020). Virtual simulation was systematically adopted in one center, while conventional sizing was used in the other one. Outcomes were the duration of intervention, the radiation dose (mGy), the number of corrective interventions for inappropriate WEB size, the number of WEBs not deployed, angiographic occlusion, and complications. Univariate and multivariate linear models were adopted.

NCT04621552
Conditions
  1. Aneurysm
  2. Intracranial Aneurysm
Interventions
  1. Device: WEB embolization
MeSH:Intracranial Aneurysm Aneurysm
HPO:Cerebral berry aneurysm Dilatation of the cerebral artery Vascular dilatation

Primary Outcomes

Description: the median duration of the intervention

Measure: Median duration of the intervention

Time: 1day

Description: the median radiation dose

Measure: Median radiation dose

Time: 1 day

Description: the need of corrective interventions

Measure: Need of corrective interventions

Time: 1 day

Description: the number of WEBs opened but finally not deployed because of the inappropriate size of the device.

Measure: number of WEBs opened

Time: 1 day

Secondary Outcomes

Description: the overall rate of complications (peri-procedural and long-term adverse events)

Measure: Overall rate of complications

Time: 1 day

Description: the morbidity rate (complications associated with permanent change of the clinical and neurological status of the patient)

Measure: morbidity rate

Time: 1 day

Description: short-term (6 months) and long-term (12 months or more) aneurysm occlusion

Measure: Rate of Aneurysm occlusion

Time: 6 months and 12 months

Description: WEB-shape change ("compaction") (decrease in height of the device or a deepening of the proximal and distal concave recesses during follow-up9 based on non-subtracted images).

Measure: WEB-shape change

Time: 6 months and 12 months

HPO Nodes


Reports

Data processed on January 01, 2021.

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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