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Anticipatory management vs standard management of postpartum haemorrhage

Not Applicable
Conditions
Postpartum haemorrhage (PPH)
Registration Number
SLCTR/2011/010
Lead Sponsor
Faculty of Medicine, Colombo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Giving birth after 36 Weeks of amenorrhea
•Post-partum haemorrhage due to uterine atony (recognized by continuing bleeding not responding to uterine massage and excluding other causes after examination)

Exclusion Criteria

•Anomalies of hemostasis before labour
•Anticoagulant treatment
•Patients with death in utero fetuses
•Diagnosed patients with placenta accreta or percreta

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
eed for use of balloon tamponade to control PPH [Until 24hours postpartum]<br>
Secondary Outcome Measures
NameTimeMethod
• Percentage of women who did not develop PPH in the standard treatment arm<br> • Need for additional intervention after initial PPH treatment<br> • Use of additional doses of oxytocin/ ergometrine<br> • Surgical interventions<br> • Compressive sutures<br> • Systematic pelvic devascularization (Uterine, Internal iliac artery ligation)<br> • Hysterectomy<br> • Change in hemoglobin from pre-delivery to postpartum<br> • Receipt of blood transfusion Need for massive blood transfusion (>5 units of blood)<br> • Maternal death [Until study subject is discharged from hospital]<br>
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