Twentyfour Ambulatory Pulse Wave Velocity and Central Augmentation Index in Type 2 Diabetes
|ClinicalTrials.gov Identifier: NCT01812811|
Recruitment Status : Completed
First Posted : March 18, 2013
Last Update Posted : December 11, 2013
|Condition or disease|
|Type 2 Diabetes|
Arteriograph24 is a new monitor for measuring ambulatory blood pressure and additional performing brachial cuff based on analysis of a suprasystolic pulse wave.
The study aim to test the feasibility of ambulatory pulse wave analysis every twenty minute (the fraction of missed measurements)and the reprodicility of pulse wave velocity and central augmentation index in type 2 diabetic patients. In addition we will explore the relation between diurnal variation of brachial blood pressure, central blood pressure and pulse wave velocity.
20 type 2 diabetic patients will have 24h ambulatory blood pressure performed twice with an interval of one week.
|Study Type :||Observational|
|Actual Enrollment :||22 participants|
|Official Title:||Twentyfour Ambulatory Pulse Wave Velocity and Central Augmentation Index in Type 2 Diabetes|
|Study Start Date :||September 2012|
|Primary Completion Date :||July 2013|
|Study Completion Date :||July 2013|
- Fraction of missed pulse wave analysis [ Time Frame: Meaured two times with an interval of one week ]Measurements of ambulatory blood pressure and pulse wave analysis is performed every twenty minute. The fraction of missed measurements of pulse wave analysis during day time and night time analysis is the final outcome
- Reproducibility of pulse wave analysis parameters [ Time Frame: Measured two times with an interval of one week ]Reproducibility of pulse wave velocity, Central systolic blood pressure and central augmentation index for 24 hour, day and night
- Diurnal variation of brachial blood pressure, central blood pressure and pulse wave velocity [ Time Frame: Measured two times with an interval of one week ]brachial blood pressure, central blood pressure and pulse wava velocity is measured evrey twenty minutes and averaged for day time and night time. the relative reduction at nioght for the parameters are calculated
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01812811
|Medical department, Diagnostic Center, Regional Hospital Silkeborg|
|Silkeborg, Denmark, 8600|
|Principal Investigator:||Klavs W Hansen, MD, dr.med.||Medical department, Diagnostic Center, Regional Hospital Silkeborg, Denmark|