← Eichor
Study identifier: NCT06646653 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

EVE TRIAL , ALMA SYSTAM

Condition: Postpartum Haemorrhage (PPH) · PPH · Postpartum Hemorrhage (Primary)  ·  Sponsor: ResQ Medical Ltd

PhasePhase 3
Planned participants50
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

abnormal bleeding after childbirth. This condition is called abnormal bleeding and becomes a condition known as postpartum hemorrhage (PPH) when worsens. Abnormal bleeding is defined as the loss of more than 500 milliliters (about two cups) of blood after a vaginal birth, or more than 1,000 milliliters (about four cups) after a cesarean section. It is a serious and potentially life-threatening complication that requires immediate medical treatment. What you need to know: * Signing this form does not mean you will have an emergency postpartum bleeding. * We will only include you in the study IF abnormal bleeding happens after your birth. * If abnormal bleeding does happen, your doctors will first try the usual treatments that work in accordance with the hospital's PPH protocol. * The study device (called Alma system) would only be used if the usual treatments do not stop the bleeding. Treatment Schedule - Recruitment \& Consenting * Screening and enrolment. * Treatment of PPH with Alma system. * Alma Survey * Follow up examination post treatment procedure (after removal of Alma system and before subject discharge from the hospital). * 6-week postpartum follow-up examination.

This description comes directly from the study's public registry record.

Talk to the study team

Yael Corcos, RN  ·  972-548106010  ·  yael@resq-med.com

Always discuss trial participation with your own doctor first.

Locations (2)

Maimonides Medical Center | Brooklyn, New York HospitalBrooklyn, New York, United StatesNot Yet Recruiting
Shaare Zedek Medical CenterJerusalem, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT06646653