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OpenTrials
Completed

NCT Number: NCT03517800

Surgical Management of Postpartum Haemorrhage Without Embolization

Postpartum haemorrhage is the main cause of maternal mortality. The aim of investigators' study was to evaluate the practice of hemostatic surgery (arterial ligation, uterine compression or hysterectomy) when the embolization of uterine arteries wasn't be performed.

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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

  • Age over 18
  • Postpartum haemorrhage
  • Necessity of second line management
  • No embolization performed
  • Necessity of surgical management after embolization

Exclusion criteria

  • Unnecessity of second line management
  • Management by only embolization
  • Incomplete medical files

Treatment and study plan

Arterial embolization and/or surgical management.

Other

Arterial embolization and/or surgical management.

Primary outcomes

  1. Frequency of each type of surgical management

    Time frame: at delivery

    Frequency of each type of surgical management

Secondary outcomes

  1. Number of surgical interventions

    Time frame: at delivery

    Number of surgical interventions

Sponsors and collaborators

Lead sponsor

University Hospital, Montpellier

Other

Registry information

Official study title

Surgical Management of Intractable Postpartum Haemorrhage When Arterial Embolization Can't be Performed : Feasibility an Complications.

Important dates

Study start
2010
Primary completion
2015
Study completion
2016
First posted
May 7, 2018
Registry last updated
May 18, 2018

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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