normal fetus
Conditions
Interventions
Intervention type:
Name of intervention:
Dose form / Japanese Medical Device Nomenclature:
Route of administration / Site of application:
Dose per administration:
Dosing frequency / Frequency of use:
Sponsors
Masahiko Nakata
Sumito Nagasaki
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: normal pregnant woman
Exclusion criteria
Exclusion criteria: Abnormal pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To construct the referential value of fetal AutoFS analysis | — |
Secondary
| Measure | Time frame |
|---|---|
| Investigate the perinatal prognosis (presence or absence of fetal fetal disease, complications of pregnancy, birth weight, abnormality of baby at birth) of pregnant women who studied and examined the relationship with Auto FS value. | — |
Countries
Japan
Contacts
Public ContactSumito Nagasaki
Toho University Omori medical center
Outcome results
None listed