Autopsy report · NCT00597545

Effect of Raised CBF During CEA on Cognition in DM Patients

Cause of deathOther Automatic label, confidence 0.3, unverified. How labels are made.

“Half of DM patients had EEG changes and therefore were excluded.”

The sponsor’s own words in the registry.

Life of this trial

Registered 10 months after it had already started.
Ran for about 7 years 3 months before it stopped.
10 participants enrolled.
Results were posted on the registry 1 year 1 month after it ended.

Vital statistics

Status: Terminated
Phase: Na
Sponsor: Columbia University
Sponsor type: University, hospital or other
Conditions: Carotid Artery Disease; Carotid Artery Stenosis; Diabetes; Cognitive Dysfunction
Interventions: Carotid endarterectomy; Shunt
Participants: 10
Sites: 1
Countries: United States

Look deeper

The official registry record (the source of truth)
Record history: every change the sponsor made
Open it in the database

Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.