A multicenter clinical study to test the efficacy and safety of C1-inhibitor concentrate for clinical amniotic fluid embolism.
Not Applicable
- Conditions
- clinical amnitotic fluid embolism
- Registration Number
- JPRN-UMIN000012273
- Lead Sponsor
- Department of Obstetrics and Gynecology, Mie university hospital.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 5
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who are anaphylactic to C1-inhibitor drug.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement of clinical symptom Improvement of laboratory data
- Secondary Outcome Measures
Name Time Method