PATTERN: Comparison of the Radiological Pattern Between the Cerebral Stroke of Arterial and Venous Origin

• Sponsor: Centre Hospitalier Universitaire, Amiens (Other)
• Overall Status: Completed
• CT.gov ID: NCT03611894
• Collaborator: (none)
• Enrollment: 98
• Locations: 2
• Actual Duration (Months): 5.9
• Patients Per Site: 49
• Patients Per Site Per Month: 8.2

Study Details

Study Description

Brief Summary

There are few published data on the patterns of parenchymal imaging abnormalities in a context of cerebral venous thrombosis (CVT). The objectives of the present study were to describe the patterns of parenchymal lesions associated with CVT and to determine the lesion sites.

Condition or Disease	Intervention/Treatment	Phase
Stroke; Superior Sagittal Sinus Thrombosis; Venous Thromboses	Other: radiological comparison

Study Design

• Study Type: Observational
• Actual Enrollment: 98 participants
• Observational Model: Case-Only
• Time Perspective: Retrospective
• Official Title: Comparison of the Radiological Pattern Between the Cerebral Stroke of Arterial and Venous Origin
• Actual Study Start Date: Jan 1, 2017
• Actual Primary Completion Date: Jul 1, 2017
• Actual Study Completion Date: Jul 1, 2017

Arms and Interventions

Arm	Intervention/Treatment
hemorrhagic ischemia comparison between clinical characteristics and the confirmed diagnosis by RMI (magnetic resonance Imaging)	Other: radiological comparison; comparison between clinical and radiological characteristics
nonhemorrhagic ischemia comparison between clinical characteristics and the confirmed diagnosis by RMI (magnetic resonance Imaging)	Other: radiological comparison; comparison between clinical and radiological characteristics
intracerebral hematoma comparison between clinical characteristics and the confirmed diagnosis by RMI (magnetic resonance Imaging)	Other: radiological comparison; comparison between clinical and radiological characteristics

Outcome Measures

Primary Outcome Measures

1. patterns [0]

   describe the patterns of parenchymal lesions associated with CVT and to determine the lesion sites.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• hospitalized patients with CVT

• parenchymal lesions on magnetic resonance imaging

Exclusion Criteria:

• No CVT

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	CHU Amiens	Amiens		France	80054
2	CHU Rouen	Rouen		France	76000

Sponsors and Collaborators

• Centre Hospitalier Universitaire, Amiens

Investigators

• Principal Investigator: Audrey Arnoux, MD, CHU Amiens

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Centre Hospitalier Universitaire, Amiens
• ClinicalTrials.gov Identifier: NCT03611894
• Other Study ID Numbers: PI2017_843_0035
• First Posted: Aug 2, 2018
• Last Update Posted: Aug 2, 2018
• Last Verified: Jul 1, 2018

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Centre Hospitalier Universitaire, Amiens: RMI
• Additional relevant MeSH terms: Stroke; Sinus Thrombosis, Intracranial; Sagittal Sinus Thrombosis; Thrombosis; Venous Thrombosis

Study Results

No Results Posted as of Aug 2, 2018