Evaluation of a translated Japanese version of ObsQoR-10
Not Applicable
- Conditions
- Cesarean &vaginal delivery
- Registration Number
- JPRN-UMIN000043032
- Lead Sponsor
- Division of Obstetric Anesthesia, Department of Anesthesiology, Saitama Medical Center, Saitama Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
- Age < 18 years - Women whose infants have died - Mother or baby requiring ICU after delivery. - Patient refusal - Inability to read or understand written Japanese - Failed neuraxial analgesia: elective cesarean delivery - General anesthesia - Intrapartum cesarean - Assisted/operative (i.e. vacuum, forceps) vaginal delivery - Previous live birth
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ObsQoR-10 Japanese version (24 hours after delivery to Day 7)
- Secondary Outcome Measures
Name Time Method EQ5D Japanese version (24 hours after delivery) Global Health Status (24 hours after delivery)