A prospective observational study on the evaluation of coagulation function of contrast medium-mixed blood using the blood coagulation analysis device TEG 6s.
Not Applicable
- Conditions
- Patients under general anesthesia with an arterial line inserted during surgery.
- Registration Number
- JPRN-UMIN000052805
- Lead Sponsor
- Tohoku University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with diseases that cause abnormalities in hemostatic coagulation ability, such as protein S/C or antithrombin deficiency, patients whose fibrinogen and platelet values deviate from the reference range in preoperative blood tests, pregnant women, patients who have difficulty obtaining consent forms, and patients who refuse consent.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method