Pattern and Management of Intracranial Cavernoma

NCT ID: NCT04181086

Last Updated: 2019-11-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

35 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-01-01

Study Completion Date

2022-01-01

Brief Summary

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Intracranial cavernous vascular malformations are variously known as cavernous angiomas, cavernous hemangiomas, or, more simply, cavernomas. Cavernomas are congenital low flow vascular lesions. It composed of irregular sinusoidal vascular channels, lacking smooth muscle, and elastic fibers. They lack feeding arteries or draining veins and contain no neural tissue. The first description of an intracranial cavernoma was given by Virchow, in 1863. For over a century, it was considered to be an extremely rare malformation, usually found at autopsy, and exceptionally diagnosed during life. The prevalence of cerebral cavernous malformations (CCM) is estimated to be 0.4-0.9%.

Detailed Description

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Conditions

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Management of Intracranial Cavernous Hemangioma

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Interventions

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surgical excision of intracranial cavernoma

microvascular excision of intracranial cavernoma

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* All patients presented with intracranial cavernomas (single or multiple, superficial or deep, supratentorial or infratentorial)
* Denovo or recurrent patients.

Exclusion Criteria

* None
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Assiut University

OTHER

Sponsor Role lead

Responsible Party

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Moataz Elshenawi

assistant lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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intracranial cavernoma

Identifier Type: -

Identifier Source: org_study_id