A prospective study on blood coagulation and fibrinolysis in the peripartum period using rotational thromboelastometry (ROTEM)
Not Applicable
Recruiting
- Conditions
- pregnancy and postpartum period
- Registration Number
- JPRN-UMIN000048160
- Lead Sponsor
- Hamamatsu University Scool of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 160
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patients medicated with antiplatelets or anticoagulants. 2. Patients who have venous thromboembolism. 3. Patients with postpartum hemorrhage during delivery (in vaginal delivery >= 800 mL, in cesarean section >= 1500 mL). 4. Patients complicated with disease involving platelets, coagulation, fibrinolysis, anticoagulation, or antifibrinolysis system. 5. Patients with anemia (hemoglobin concentration <8.0 g/dL) before the delivery. 6. Patients with severe liver disease (or AST >= 100 U/L). 7. Patients with severe renal disease (or serum creatinine >= 1.3 mg/dL).
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method