Ignite Creation Date:
2024-05-05 @ 12:05 PM
Last Modification Date:
2024-10-26 @ 9:20 AM
Study NCT ID:
NCT00235846
Status:
COMPLETED
Last Update Posted:
2015-04-14
First Post:
2005-10-10
Brief Title:
Endoscopic Vessel Harvesting During Coronary Bypass Surgery
Sponsor:
Aalborg University Hospital
Organization:
Aalborg University Hospital
Study Overview
Official Title:
Endoscopic Vessel Harvesting During Coronary Bypass Surgery
Status:
COMPLETED
Status Verified Date:
2015-04
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:
Conventional open vein harvesting from the legs during coronary artery bypass surgery result in wound complications among 30 of the patients Endoscopic harvesting decrease the complication rate but it remains to be shown whether this is also a fact among patient in whom only short segments of veingraft material is needed from the leg We hypothesise that the rate of wound complications will be reduced and the patient satisfaction will be increased also among patients in whom only short vein segments are endoscopically harvested compared to conventional open vein harvesting
Detailed Description:
Conventional open vein harvesting from the legs during coronary artery bypass surgery result in wound complications among 30 of the patients Endoscopic harvesting decrease the complication rate but it remains to be shown whether this is also a fact among patient in whom only short segments of veingraft material is needed from the leg We hypothesise that the rate of wound complications will be reduced and the patient satisfaction will be increased also among patients in whom only short vein segments are endoscopically harvested compared to conventional open vein harvesting
Preoperative demographic as well ass peri- and postoperative data are collected prospectively at 5-7 days and 1 month postoperatively Wound complications are registered as well as post operative pain in the wound is evaluated using af visual analogue scale Patients are evaluating the cosmetic results after wound healing
Preoperative demographic as well ass peri- and postoperative data are collected prospectively at 5-7 days and 1 month postoperatively Wound complications are registered as well as post operative pain in the wound is evaluated using af visual analogue scale Patients are evaluating the cosmetic results after wound healing
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