Ignite Creation Date:
2024-05-06 @ 1:46 PM
Last Modification Date:
2024-10-26 @ 1:19 PM
Study NCT ID:
NCT04111744
Status:
COMPLETED
Last Update Posted:
2019-10-01
First Post:
2018-03-21
Brief Title:
Preoperative Excercise Training for Patients Undergoing Coronary Artery Bypass Graft Surgery
Sponsor:
Kerckhoff Klinik
Organization:
Kerckhoff Klinik
Study Overview
Official Title:
Preoperative Excercise Training for Patients Undergoing Coronary Artery Bypass Graft Surgery- A Prospective Randomized Trial
Status:
COMPLETED
Status Verified Date:
2019-09
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:
None
Brief Summary:
Patients pts with stable coronary artery disease CAD requiring coronary artery bypass graft surgery CABG may be physically inactive during the waiting period to avoid further risks Aim of this study is to investigate the feasibility and safety of a preoperative aerobic exercise training in these pts during the waiting period and to analyze its effects on pre- peri and postoperative outcomes
Detailed Description:
Pts with stable coronary artery disease CAD and indication for elective CABG will be prospectively randomized into a preoperative training group TG or a non active control group CG Pts in TG have to perform six sessions of aerobic endurance training within two weeks prior to CABG The following investigations will be performed at baseline one day before surgery and at the beginning and at the end of cardiac rehabilitation a maximal symptom limited ergospirometry assessment of endothelial function analysing the reactive hyperaemic index RHI via a finger-tonometry assessment of quality of life QoL using the MacNew Heart Disease Questionnaire laboratory testing of ischemic and inflammatory Parameters Baseline peri- and postoperative characteristics will be collected
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None