Tampostat for Management of Postpartum Hemorrhage
Postpartum Hemorrhage
About this trial
This is an interventional treatment trial for Postpartum Hemorrhage focused on measuring Tampostat, Tamponade, Postpartum hemorrhage
Eligibility Criteria
Inclusion Criteria:
- Women who delivered their baby at the site hospital, or attended the site hospital with PPH that started within the last 24 hours.
- Women with primary PPH have received AMTSL.
- PPH is due to atonic uterus.
- Provides written informed consent for enrolment in the study.
Exclusion Criteria:
- Primary PPH caused by retained placenta or ruptured uterus.
- Women who delivered before 28 weeks of gestation.
- Women not willing to participate in the study.
Sites / Locations
- Obstetrical Ward of Shaheed Suhrawardi Medical College Hospital (ShSMCH) and Dhaka Medical College Hospital (DMCH)
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Tampostat
Condom catheter tamponade
Tampostat™ is a self-regulating, low cost, pressure based emergency obstetric device designed specifically for use in low-resource settings. It has 6 parts: probe, condom, O ring, nerve centre, tube and bulb pump. It offers significant benefits over the current model by simplifying the insertion process, reducing the need for constant monitoring, eliminating leakage and the need for sterile saline, and using a pressure-based mechanism to apply consistent pressure to all women regardless of uterus size.Women who develop PPH even after applying AMTSL at the hospital or women who visit the hospital with PPH within 24 hours after delivery will be managed by Tampostat for the intervention arm or by the condom catheter tamponade in the control arm(172 patients in each arm)
Condom catheter tamponade have been used by medical professionals for several years in the management of atonic (primary) PPH. In this approach, Sterile rubber catheter fitted with a condom as a tamponade balloon device and using normal saline to inflate the condom.