The Effect of Different Delivery Positions on Pelvic Floor Function.

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age20-35
SponsorPeking University People's Hospital

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

This trial accepts healthy volunteers

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 population

Singleton, cephalic position, full-term primipara aged 20-35 years old without cephalopelvic disproportion, expected fetal weight ≥ 4000gpelvic floor organ prolapse beyond the hymen limbus and combined with uncontrolled medical diseases and asthma, allergic rhinitis and constipation before pregnancy.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Lithotomy position

    Behavioral

    Participants in the lithotomy decubitus position group were in the lithotomy position at the second stage of labor of delivery.

  • Lateral Position

    Behavioral

    Participants in the lateral position group were in the lateral position at the second stage of labor of delivery.

  • Upright Position

    Behavioral

    Participants in the upright position group were in the upright position at the second stage of labor of delivery.

Treatment groups

669 Participants
are divided into 3 treatment groups
Group A: Lithotomy Position Group1 intervention
Group B: Upright Position Group1 intervention
Group C: Lateral Position.1 intervention

Trial outcomes

Primary outcomes

1

Stress urinary incontence (SUI) occurrence at 6 weeks postpartum

Time frame
at 6 (±1) weeks postpartum

Secondary outcomes

Other outcomes

Sponsors and contacts

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