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OpenTrials
Completed

NCT Number: NCT04566705

Uterine Rupture During Labor Among Women With a Prior Cesarean Delivery

Although a rare event, uterine rupture during labour is one of the most serious obstetric complications because of the dramatic maternal-fetal consequences that can result.

Identifying the risk factors associated with uterine rupture would enable gynecologists to provide patients with risks of uterine rupture in the event of attempted vaginal delivery.

The aim of our study is to determine risks factors for uterine rupture during labour in patients with a previous cesarean delivery who have not given birth since and to assess the occurrence of maternal-fetal comply-cations compared to patients with a previous cesarean delivery without uterine rupture.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Singleton pregnancy > 24 weeks of gestation
  • Second or multiparous with a previous cesarean section without vaginal delivery since
  • Cephalic presentation or completed breech
  • Uterine rupture during labor

Exclusion criteria

  • Incomplete uterine rupture
  • Multiple gestation
  • Transverse presentation or complete breech
  • Vaginal delivery after cesarean
  • Non-low transverse cesarean section
  • Placenta praevia
  • Antepartum intrauterine fetal death
  • History of uterine surgery (myomectomy)

Treatment and study plan

Risks factors, maternal and neonatal outcomes/complications

Other

Risks factors, maternal and neonatal outcomes/complications

Primary outcomes

  1. Assess the risks factors of uterine rupture

    Time frame: 1 day

    Assess the risks factors of uterine rupture

    Assess the risks factors of uterine rupture using obstetric measures

Secondary outcomes

  1. Number of Participants with Assess the maternal and perinatal complications and outcomes

    Time frame: 1 day

    Number of Participants withAssess the maternal and perinatal complications and outcomes : looking for maternal complications (chorioamnionitis , transfusion, post-partum hemorrhage, surgery for blad-der wound, maternal death,…) and neonatal comply-cations (apgar<7 at 5minutes, pH <7,15, neonatal intein-sive care unit and perinatal death)

Sponsors and collaborators

Lead sponsor

University Hospital, Montpellier

Other

Registry information

Official study title

Uterine Rupture During Labor Among Women With a Prior Cesarean Delivery : Risks Factors, Maternal and Perinatal Outcomes

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Sep 28, 2020
Registry last updated
Nov 18, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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