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Study of Predictors of Failure of Sulprostone Treatment in Postpartum Hemorrhage (NALAPOST)

U

University Hospital, Strasbourg, France

Status

Completed

Conditions

Postpartum Hemorrhage

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The investigators wish to identify potential factors predicting failure of second-line drug treatment (sulproston (Nalador®)): risk factors and factors linked to a failure to take initial care for PPH.

A better understanding of the aggravating factors of HPP and more particularly the factors inherent to the initial care would make it possible to think of ways to improve practices.

Enrollment

300 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Major subject (≥18 years old)
  • Subject having given birth at HUS or CHU Poissy Saint-Germain-en Laye between 01/01/2019 and 31/12/2020
  • Subject having presented a postpartum haemorrhage treated with Sulprostone
  • Subject not having expressed his opposition, after information, to the reuse of his data for the purposes of this research

Exclusion criteria

  • Subject having expressed opposition to participating in the study
  • Subject under guardianship or guardianship
  • Subject under safeguard of justice

Trial contacts and locations

1

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Central trial contact

Saïd CHAYER, PhD, HDR; Sandrine VOILLEQUIN, Midwife

Data sourced from clinicaltrials.gov

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