Phase
Condition
Uterine Disorders
Hemorrhage
Treatment
KOKO Device
Clinical Study ID
Ages > 18 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Adult Female, 18 years of age or older at time of consent.
Subject is able to understand and provide informed consent to participate in thestudy.
Diagnosis of abnormal postpartum uterine bleeding (500 - 999 ml for vaginal birth)or postpartum hemorrhage (1000 - 1500 ml for vaginal or Cesarean birth) withsuspected atony within 24 hours after vaginal or cesarean birth.
EBL, to be determined when investigator is ready to have the KOKO packaging opened:Vaginal birth: 500 - 1500 ml EBL or Cesarean birth: 1000 - 1500 ml EBL.
Failed first - line intervention of uterotonics and uterine massage/bimanual uterinemassage to stop bleeding. Note: Uterotonic administration may continue concomitantwith and post KOKO use.
Exclusion
Exclusion Criteria:
EBL >1500ml, to be determined when investigator is ready to have the KOKO packagingopened.
Delivery at a gestational age < 34 weeks or, if multiples, uterus is judged <34weeks size.
For cesarean births: Cervix < 2.5 cm dilated before use of KOKO.
Abnormal postpartum uterine bleeding or hemorrhage that the investigator determinesto require more aggressive treatment, including any of the following:
hysterectomy;
B-lynch suture;
uterine artery embolization or ligation;
hypogastric ligation.
Known uterine anomaly.
Ongoing intrauterine pregnancy.
Placental abnormality including any of the following:
known placenta accreta;
retained placenta with known risk factors for placenta accreta (e.g., historyof prior uterine surgery, including prior cesarean and placenta previa);
retained placenta without easy manual removal.
Known uterine rupture.
Unresolved uterine inversion.
Subject has undergone intrauterine balloon therapy, uterine packing or use of othernegative pressure system(s) for tamponade treatment of this episode of abnormalpostpartum uterine bleeding or hemorrhage prior to use of the KOKO™ device.
Current cervical cancer.
Current purulent infection of vagina, cervix, uterus.
Diagnosis of coagulopathy.
Study Design
Study Description
Connect with a study center
University of Alabama
Birmingham, Alabama 35233
United StatesActive - Recruiting
Christiana Care
Newark, Delaware 19718
United StatesActive - Recruiting
Indiana University School of Medicine, Dept. of OBGYN
Indianapolis, Indiana 46202
United StatesActive - Recruiting
Ochsner Baptist
New Orleans, Louisiana 70115
United StatesActive - Recruiting
New York-Presbyterian Hospital (NYPH)/Columbia University Irving Medical Center (CUIMC)
New York, New York 10032
United StatesActive - Recruiting
Cleveland Clinic (Fairview)
Cleveland, Ohio 44111
United StatesSite Not Available
MetroHealth
Cleveland, Ohio 44109
United StatesSite Not Available
The Cleveland Clinic
Cleveland, Ohio 44111
United StatesActive - Recruiting
The Ohio State University
Columbus, Ohio 43210
United StatesActive - Recruiting
University of Utah
Salt Lake City, Utah 84132
United StatesActive - Recruiting
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