Safety and Effectiveness of the Jada System in Treating Primary Postpartum Hemorrhage
The purpose of this study is to evaluate the safety and effectiveness of the InPress Device in the control and reduction of primary postpartum hemorrhage.
- Postpartum Hemorrhage
- Eligible Ages
- Over 18 Years
- Eligible Genders
- Accepts Healthy Volunteers
- Adult Female, 18 years of age or older at time of consent.
- Able to understand and provide informed consent to participate in the study.
- Diagnosis of PPH with suspected atony within 24 hours after vaginal or c-section delivery.
- EBL, to be determined when investigator is ready to have InPress Device peel pack opened: a) vaginal delivery: 500 - 1500 ml EBL or b) c-section delivery: 1000 - 1500 ml EBL.
- Failed first-line intervention of uterotonics and uterine massage/bimanual compression to stop bleeding. Note: Pitocin administration may continue concomitant with and post InPress Device use.
- EBL > 1500 ml, to be determined when investigator is ready to have the InPress Device peel pack opened.
- Delivery at a gestational age < 34 weeks.
- For C-sections: Cervix < 3 cm dilated before C-section.
- PPH that the investigator determines to require more aggressive treatment, including any of the following: a) hysterectomy, b) b-lynch suture, c) uterine artery embolization or ligation, d) hypogastric ligation.
- Known uterine anomaly.
- Ongoing intrauterine pregnancy.
- Placenta abnormality including any of the following: a) known placenta accreta, b) retained placenta with known risk factors for placenta accreta (e.g. history of prior uterine surgery, including prior c-section and placenta previa), c) retained placenta without easy manual removal.
- Known uterine rupture.
- Unresolved uterine inversion.
- Subject has undergone intrauterine balloon therapy or uterine packing for tamponade treatment of this PPH prior to use of the InPress Device.
- Current cervical cancer.
- Current purulent infection of the vagina, cervix, uterus.
- Diagnosis of coagulopathy.
- Study Type
- Intervention Model
- Single Group Assignment
- Primary Purpose
- None (Open Label)
|Jada System for Postpartum Hemorrhage will be administered to subjects who are diagnosed with postpartum hemorrhage.||
- NCT ID
- Alydia Health
Study ContactKathryn D Wine, MPH
This IDE study is designed to evaluate the effectiveness and safety of the InPress Device to treat primary PPH. The study is literature controlled.