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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01919775
Other study ID # tohoku-ACoA amnesia MRI
Secondary ID
Status Completed
Phase N/A
First received August 7, 2013
Last updated August 7, 2013
Start date December 2007
Est. completion date July 2013

Study information

Verified date August 2013
Source Tohoku University
Contact n/a
Is FDA regulated No
Health authority Japan: Institutional Review Board
Study type Observational [Patient Registry]

Clinical Trial Summary

To clarify whether amnesia after treatment of anterior communicating aneurysm (ACoA)is related to infarcts caused by occlusion or damage of the perforating artery of the ACoA, we used 3.0-T 3D high resolution MR imaging to identify and localize infarcts in patients with amnesia following treatment of ACoA aneurysm.


Description:

Cohort register is made by experienced neuropsychologists in our institute.

MR imaging and data storage is in the department of diagnostic radiology of our institute.

MR images are evaluated by two neuroradiologists using a work station.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date July 2013
Est. primary completion date July 2013
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

Clinical diagnosis of Amnesia

Exclusion Criteria:

Severe decreased intellectual function

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Tohoku University

Outcome

Type Measure Description Time frame Safety issue
Primary cerebral infarction identified and localized in the basal forebrain on MR imaging within 15 months from the aneurysmal treatment(an expected average 4 months) No
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