Ignite Creation Date:
2024-05-05 @ 4:50 PM
Last Modification Date:
2024-10-26 @ 9:24 AM
Study NCT ID:
NCT00324350
Status:
COMPLETED
Last Update Posted:
2012-10-05
First Post:
2006-05-10
Brief Title:
Intensive Glycemic Control and Skeletal Health Study
Sponsor:
University of California San Francisco
Organization:
University of California San Francisco
Study Overview
Official Title:
Intensive Glycemic Control and Skeletal Health Study - Ancillary Study to the Action to Control Cardiovascular Risk in Diabetes Trial ACCORD-BONE
Status:
COMPLETED
Status Verified Date:
2012-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
ACCORD-BONE
Brief Summary:
The purpose of the ACCORD-BONE Study is to investigate the effects of intensive glycemic control for type 2 diabetes in ACCORD participants on factors related to bone health including fractures falls and bone mineral density
Detailed Description:
Recent studies have established that type 2 diabetes is a risk factor for fractures particularly of the hip shoulder and foot Additionally type 2 diabetes is associated with a 50-60 increase in the risk of falling The higher risk of fracture associated with type 2 diabetes is an important health burden for these patients More frequent falls and perhaps reduced bone strength in those with diabetes are thought to be key contributing factors The best approach to preventing fractures in type 2 diabetes is not yet understood There is observational evidence to support our hypothesis that better glycemic control will preserve bone and reduce falls and fractures The ACCORD-BONE study provides a unique opportunity to determine whether intensive glycemic control will prevent fractures falls and bone loss in older diabetic adults which may lead to improved treatment and prevention in the future
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None