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NCT00700674 Clinical Trial

Effect of Usage of Electroencephalogram (EEG) Entropy on the Incidence of Postoperative Cognitive Dysfunction in Geriatric Patients

Cognitive Dysfunction Clinical Trial

Official title:
Is the Ese of EEG Entropy as Intra-operative Monitor Improves Postoperative Cognitive Dysfunction

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00700674
Other study ID # RP 0729
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date January 2008
Est. completion date November 2011

Study information
Verified date February 2010
Source King Khaled Eye Specialist Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To determine if the usage of EEG Entropy helps to reduces the incidence of POCD in elderly patients after general anesthesia.

Recruitment information / eligibility
Status Terminated
Enrollment 60
Est. completion date November 2011
Est. primary completion date November 2011
Accepts healthy volunteers No
Gender All
Age group 60 Years to 75 Years
Eligibility Inclusion Criteria: - ASA physical status I-II. - scheduled for retinal surgery expected to take 2-3 hours under general anesthesia. - orotracheal intubation. Exclusion Criteria: - history of cardiac, pulmonary, liver or renal disease. - significant obesity (body mass index >30. - Long-term user of central nervous system activator drugs, benzodiazepines and/or opiates. - dementia, brain atrophy and other neurological disorder.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Saudi Arabia King Khaled Eye Specialist hospital Riyadh

Sponsors (1)
Lead Sponsor Collaborator
King Khaled Eye Specialist Hospital

Country where clinical trial is conducted

Saudi Arabia, 

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