About this trial
This study is a cohort clinical study. Baseline data were collected from cases recruited at pregnancy, and the eligible subjects were grouped into 3 groups according to different delivery position including supine position group, upright position group, and lateral position group. Different delivery positions along with respectively timeand obstetric conditions were recorded at delivery. Pelvic floor function assessments were performed at postpartum.
Eligibility criteria
Qualifiers
Age 20-35 years old
Singleton, cephalic position, full-term primipara;
Cephalopelvic disproportion;
Expected fetal weight< 4000g;
Disqualifiers
Pelvic floor organ prolapse beyond the hymen limbus;
Combined with uncontrolled medical diseases and asthma, allergic rhinitis and constipation before pregnancy;
Presence of contraindications to vaginal delivery
Trial design
Treatments tested in this trial
- Lithotomy position
- Lateral Position
- Upright Position