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Anticipatory management vs standard management of postpartum haemorrhage

Anticipatory management vs standard management of postpartum haemorrhage

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
SLCTR
Registry ID
SLCTR/2011/010
Enrollment
Unknown
Registered
2011-07-25
Start date
2011-07-31
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum haemorrhage (PPH)

Interventions

Intervention group will receive anticipatory management protocol while the control group will receive standard management protocol. Standard management. If visually assessed blood loss is ? 500ml or

Sponsors

Faculty of Medicine, Colombo
Lead Sponsor

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Need for use of balloon tamponade to control PPH [Until 24hours postpartum]

Secondary

MeasureTime frame
• Percentage of women who did not develop PPH in the standard treatment arm • Need for additional intervention after initial PPH treatment • Use of additional doses of oxytocin/ ergometrine • Surgical interventions • Compressive sutures • Systematic pelvic devascularization (Uterine, Internal iliac artery ligation) • Hysterectomy • Change in hemoglobin from pre-delivery to postpartum • Receipt of blood transfusion Need for massive blood transfusion (>5 units of blood) • Maternal death [Until study subject is discharged from hospital]

Countries

Sri Lanka

Contacts

Public ContactProf. Hemantha Senanayake
senanayakeh@gmail.com0112556340

Outcome results

None listed

Source: SLCTR (via WHO ICTRP) · Data processed: Aug 9, 2026