Early Detection of Cognitive Dysfunction in Diabetes
Study of Cognitive Dysfunction and Diabetes
1 other identifier
observational
400
1 country
3
Brief Summary
The rate of cognitive decline due to ageing is increased 1.5-fold to 2.0-fold in individuals with type 2 diabetes.There are no established specific treatment measures to prevent or ameliorate cognitive impairments in patients with diabetes. we want to detecte early clinical dementia in diabete.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2012
Typical duration for all trials
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2012
CompletedFirst Submitted
Initial submission to the registry
April 1, 2013
CompletedFirst Posted
Study publicly available on registry
April 12, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2014
CompletedDecember 10, 2014
December 1, 2014
2.9 years
April 1, 2013
December 9, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
MMSE Olfactory function dementia
MMSE,Olfactory function and PET(fMRI) were observed.
2 years
Study Arms (4)
control,MCI, Olfactory dsfunction
There are different groups:control,MCI, Olfactory dsfunction.
control, MCI
control and MCI group.Glycaemic control
control and MCI
treatment and without treatment
MCI and Olfactory function
observation between MCI and Olfactory function groups.
Eligibility Criteria
Patients with type 2 diabetes
You may qualify if:
- Patients with type 2 diabetes(Age\>50 years)
You may not qualify if:
- with stroke or other complications.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (3)
Wuhan general hospital of Guangzhou Command
Wuhan, Hubei, 430070, China
tongji Medical University
Wuhan, Hubei, 430074, China
Wuhan general hospital of Guangzhou command
Wuhan,chongqing, Hubei, 430070, China
Biospecimen
serum
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- doctor
Study Record Dates
First Submitted
April 1, 2013
First Posted
April 12, 2013
Study Start
January 1, 2012
Primary Completion
December 1, 2014
Study Completion
December 1, 2014
Last Updated
December 10, 2014
Record last verified: 2014-12