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Clinical Trials/ISRCTN14141270
ISRCTN14141270
Completed
N/A

A randomised controlled trial of educational counseling on the management of women who have suffered suboptimal outcomes during childbirth

Hong Kong Health Services Research Fund (Hong Kong)0 sites180 target enrollmentOctober 9, 2002

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Hong Kong Health Services Research Fund (Hong Kong)
Enrollment
180
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 9, 2002
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Hong Kong Health Services Research Fund (Hong Kong)

Eligibility Criteria

Inclusion Criteria

  • Parturients who developed suboptimal outcomes during pregnancy. Suboptimal outcomes are defined as:
  • 1\. Perinatal deaths (intra\-uterine death, stillbirth and neonatal death)
  • 2\. Treatment in the neonatal intensive care unit and special care unit
  • 3\. Unexpected obstetric events, which include significant antenatal complications, such as hypertension and ante\-partum haemorrhage, and intra\-uterine and post\-partum events, such as emergency caesarean deliveries, operative vaginal deliveries and haemorrhage

Exclusion Criteria

  • Does not meet exclusion criteria

Outcomes

Primary Outcomes

Not specified

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