ClinicalTrials.gg
CompletedNCT01919775Updated Aug 9, 2013

Amnesia After Surgery for Anterior Communicating Aneurysm: High Resolution Magnetic Resonance (MR) Imaging Findings

An observational study in Subarachnoid Hemorrhage, Cerebral Aneurysm and Amnesia, sponsored by Tohoku University. Completed. Per ClinicalTrials.gov, last updated 2013-08-09.

Sponsored by Tohoku University · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
14
Sex
All
01

Study 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.

Read the detailed 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.

02

Conditions studied

  • Subarachnoid Hemorrhage
  • Cerebral Aneurysm
  • Amnesia
03

In context

Subarachnoid Hemorrhage

510 studies on the registry are indexed under Subarachnoid Hemorrhage; 128 are open to participants now.

This study's enrollment of 14 is below the median of 120 across 226 observational studies indexed under Subarachnoid Hemorrhage.

Browse Subarachnoid Hemorrhage studies →

Lead sponsor

Tohoku University is the lead sponsor of 8 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients with amnesia following surgical treatment of the ACoA aneurysm.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Clinical diagnosis of Amnesia

Exclusion criteria

Exclusion Criteria:

Severe decreased intellectual function

05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
14 participants (actual)
Target follow-up
6 Years
Patient registry
Yes
06

What researchers measure

Primary outcomes

  1. cerebral infarction identified and localized in the basal forebrain on MR imaging

    Time frame: within 15 months from the aneurysmal treatment(an expected average 4 months)

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 9, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01919775
Lead sponsor
Tohoku University
Responsible party
Shunji MUGIKURA (Principal Investigator, Associate professor of Departmetn of Diagnostic radiology, Tohoku University) — Principal investigator
First posted
Aug 9, 2013
Start date
Dec 2007
Primary completion
Jul 2013
Completion
Jul 2013
Last update
Aug 9, 2013

Study contacts

Shoki Takahashi, Professor
study director · Department of Diagnostic Radiology, Tohoku University, Graduate School of Medicine, Sendai, Japan

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2013. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion