Postpartum uterine involution
Conditions
Interventions
Low-Intensity Pulsed Focused Ultrasound (LIPUS):The LIPUS group underwent therapy with a Model-CKC100 Ultrasound Therapeutic Device for Utero Involution
Control group:The control group received uterine involution supportive treatment. For the parturients, the same equipment was used and the operation method was the same as that of the treatment group.
Sponsors
The First Affiliated Hospital of Chongqing Medical University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Pregnant women with a gestational age of 37 weeks or more, without severe prenatal complications, willing to follow the prescribed breastfeeding and postpartum exercise plans, and planning to have a vaginal delivery.
Exclusion criteria
Exclusion criteria: Placenta previa, intrahepatic cholestasis of pregnancy, multiple pregnancies, macrosomia, polyhydramnios, a history or evidence of placental abruption, severe preeclampsia, and pregnant women who plan to undergo cesarean section.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Uterine volume reduction rate;fundal height; | — |
Secondary
| Measure | Time frame |
|---|---|
| puerperal infection;duration of lochia; | — |
Countries
China
Contacts
Public ContactLuo Xin
The First Affiliated Hospital of Chongqing Medical University
Outcome results
None listed