Temporary Aortic Compression With the Abdominal Tourniquet for Refractory Postpartum Hemorrhage
Recruiting
N/A
Interventional Study
Postpartum Hemorrhage
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 50
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 20 (estimated)
- Sponsor
- LLC UkrMedGroup · Industry
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About This Trial
This multicenter study aims to evaluate effectiveness and safety of using the AAJT-S device as a temporary intervention for severe, atony-related PPH that is refractory to standard therapies
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age ≥18 years
* Clinical diagnosis of postpartum hemorrhage (PPH) refractory to uterotonics and intrauterine balloon tamponade
* Estimated blood loss greater than 1300 mL
* Oral informed consent provided prior to device application
Exclusion Criteria:
* Patients with postpar…
Contacts