Invasive interventional study on the effectiveness of Hydroxyprogesterone caproate for pregnant women with previous spontaneous miscarriage or premature birth
Not Applicable
- Conditions
- threatened miscarriage threatened premature labor
- Registration Number
- JPRN-UMIN000028518
- Lead Sponsor
- Gunma University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 0
Inclusion Criteria
Not provided
Exclusion Criteria
1) Women with artificial abortion or premature birth 2) Patients with bleeding tendency 3) Dialysis patients 4) Patients with severe mental illness 5) Severe diabetic patients with HbA1c(NGSP)>10% 6) Other patients who are inappropriate for the study according to the judgement of the doctor
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method