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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: TCTR
Last refreshed on: 1 April 2024
Main ID:  TCTR20140901001
Date of registration: 01/09/2014
Prospective Registration: No
Primary sponsor: government
Public title: Use of brain perfusion SPECT to determine responder to choline esterase inhibitor to reduce national therapeutic cost
Scientific title: Use of brain perfusion SPECT to determine responder to choline esterase inhibitor to reduce national therapeutic cost
Date of first enrolment: 01/05/2014
Target sample size:
Recruitment status: Completed
URL:  https://www.thaiclinicaltrials.org/show/TCTR20140901001
Study type:  Observational
Study design:  N/A  
Phase:  Phase 4
Countries of recruitment
THAILAND
Contacts
Name: Supatporn    Tepmongkol
Address:  Division of Nuclear Medicine, Department of Radiology, Faculty of Medicine, Chulalongkorn University 10330 Bangkok Thailand
Telephone: 022564283
Email: supatporn@hotmail.com
Affiliation:  Faculty of Medicine, Chulalongkorn University
Name: Supatporn    Tepmongkol
Address:  Division of Nuclear Medicine, Department of Radiology, Faculty of Medicine, Chulalongkorn University 10330 Bangkok Thailand
Telephone: 022564283
Email: supatporn@hotmail.com
Affiliation:  Faculty of Medicine, Chulalongkorn University
Key inclusion & exclusion criteria
Inclusion criteria: Diagnosis of probable Alzheimer's disease by NINCDS/ADRDA criteria, mild to moderate degree
Exclusion criteria: Severe head trauma, delirium, depression, other known neuro-psychologic diseases, COPD, asthma, sik sinus syndrome, ischemic heart disease, peptic ulcer, history of gastrointestinal bleeding, type I DM, had received choline esterase inhibitors or nicergoline or other research drugs within 1 month before the study, alcohol or drug abuse, during treatment with NSAIDs, anticholinergic, carrbamazepine, dexamethasone, phenobarbital, ketoconazole

Age minimum: 50 Years
Age maximum: 0 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Alzheimer's disease
Alzheimer's disease response to donepezil
Alzheimer's disease
Intervention(s)
Screening
mild to moderate Alzheimer's disease
Primary Outcome(s)
cognitive function 0,3,6 months cognitive battery tests
Secondary Outcome(s)
brain perfusion SPECT change 0,4 hr, 15 days, 3 months brain perfusion SPECT
Secondary ID(s)
Source(s) of Monetary Support
government
Secondary Sponsor(s)
Ethics review
Status:
Approval date:
Contact:
Results
Results available:
Date Posted:
Date Completed: 01/09/2014
URL:
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