intrauterine fetal death and mid-term abortion
Conditions
Interventions
After obtaining consent from the patient, the patient will be randomly assigned to receive propofol or dexmedetomidine. Intervention begins when a labor attack appears. Start administration of both pr
Sponsors
Kimizuka Motonobu
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Patients who delivered due to intrauterine fetal death and mid-term abortion at our hospital
Exclusion criteria
Exclusion criteria: a history of allergies to propofol, dexmedetomidine, or fentanyl, contraindication for propofol or dexmedetomidine, or do not consent to the patient.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of depression by BDI-II | — |
Secondary
| Measure | Time frame |
|---|---|
| Narcotic use, sedation / analgesia scoring, delivery time, patient respiratory and circulatory dynamics, bleeding volume, presence or absence of complications | — |
Contacts
Public ContactMotonobu Kimizuka
Department of Anesthesiology
Outcome results
None listed