Methods for early detection of postpartum haemorrhage: a randomized control trial.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR202405587087519

Enrollment

220

Registered

2024-05-31

Start date

2024-05-20

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

Pregnancy and Childbirth

Interventions

calibrated BRASS V drape

Maternawell tray for monitoring of postpartum blood loss

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: ? > 18 years old ? Vaginal delivery anticipated

Exclusion criteria

Exclusion criteria: ? Refusal of informed consent ? Anticipated vaginal delivery abandoned ? Significant medical or obstetric complications

Design outcomes

Primary

Measure	Time frame
Satisfaction of study participants	—

Secondary

Measure	Time frame
Early detection of post partum hemorrhage	—

Countries

South Africa

Contacts

Public ContactMandisa Singata Madliki

Director Effective Care Research Unit

mandisa.singata@gmail.com0824201743

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026