Endovascular Repair of Aortic Aneurysm Clinical Trial
Official title:
Comparison of Intravenous Anesthetics and Volatile Anesthetics on Postoperative Cognitive Dysfunction of Patients Undergoing Endovascular Repair of Aortic Aneurysm and Endovascular Treatment of Arteriosclerosis Obliterans of Lower Extremities.
NCT number | NCT02107170 |
Other study ID # | VIAEV |
Secondary ID | |
Status | Completed |
Phase | Phase 4 |
First received | |
Last updated | |
Start date | February 2014 |
Est. completion date | December 2017 |
Verified date | June 2018 |
Source | First Affiliated Hospital, Sun Yat-Sen University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Endovascular repair of aortic aneurysm and endovascular treatment of arteriosclerosis obliterans of lower extremities are two kinds of common surgeries in the investigators' hospital. The effects of anesthetic agents on postoperative outcome, especially cognitive function, are not clear. In this study investigators propose to measure postoperative cognitive function and other outcome of patients who are undergoing these two kinds of surgeries, and try to identify whether there is an association between different kinds of anesthetics and postoperative outcome. Investigators will also observe whether changes in plasma levels of VEGF, TGF-1, TNF-α, IL-1β, and IL-6, are associated with postoperative delirium or cognitive change.
Status | Completed |
Enrollment | 68 |
Est. completion date | December 2017 |
Est. primary completion date | October 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 100 Years |
Eligibility |
Inclusion Criteria: - age 18-100 years of age - Patients presenting for Endovascular repair of aortic aneurysm and endovascular treatment of arteriosclerosis obliterans of lower extremities Exclusion Criteria: - Patients with pre-existing delirium - Inablility to converse |
Country | Name | City | State |
---|---|---|---|
China | First Affiliated Hospital, Sun Yat-Sen University | Guangzhou | Guangdong |
Lead Sponsor | Collaborator |
---|---|
Tao Zhang |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of patients with postoperative cognitive dysfunction | 7 days after surgery | ||
Secondary | Number of patients with postoperative cognitive dysfunction | 3 months after surgery | ||
Secondary | Changes in plasma levels of VEGF, TGF-1, TNF-a, IL-1ß, and IL-6 (a composite outcome measure) | 3 days after surgery |