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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03517800
Other study ID # RECHMPL17_0259
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2010
Est. completion date October 1, 2016

Study information

Verified date October 2017
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 716
Est. completion date October 1, 2016
Est. primary completion date December 1, 2015
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 44 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Arterial embolization and/or surgical management.
Arterial embolization and/or surgical management.

Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Frequency of each type of surgical management Frequency of each type of surgical management at delivery
Secondary Number of surgical interventions Number of surgical interventions at delivery
See also
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