Phase
Condition
Hemorrhage
Uterine Disorders
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
University of Alabama
Birmingham 4049979, Alabama 4829764 35233
United StatesSite Not Available
Christiana Care
Newark, Delaware 19718
United StatesActive - Recruiting
Christiana Care
Newark 4143861, Delaware 4142224 19718
United StatesSite Not Available
University of Miami
Miami, Florida 33136
United StatesActive - Recruiting
University of Miami
Miami 4164138, Florida 4155751 33136
United StatesSite Not Available
Indiana University School of Medicine, Dept. of OBGYN
Indianapolis, Indiana 46202
United StatesActive - Recruiting
Indiana University School of Medicine, Dept. of OBGYN
Indianapolis 4259418, Indiana 4921868 46202
United StatesSite Not Available
University of Kentucky
Lexington, Kentucky 40536
United StatesSite Not Available
University of Kentucky
Lexington 4297983, Kentucky 6254925 40536
United StatesSite Not Available
Ochsner Baptist
New Orleans, Louisiana 70115
United StatesSite Not Available
LSU Heath Sciences Center - Shreveport
Shreveport, Louisiana 71103
United StatesActive - Recruiting
Ochsner Baptist
New Orleans 4335045, Louisiana 4331987 70115
United StatesSite Not Available
LSU Heath Sciences Center - Shreveport
Shreveport 4341513, Louisiana 4331987 71103
United StatesSite Not Available
Sunrise Hospital and Medical Center
Las Vegas, Nevada 89109
United StatesActive - Recruiting
Sunrise Hospital and Medical Center
Las Vegas 5506956, Nevada 5509151 89109
United StatesSite Not Available
New York-Presbyterian Medical Group Queens
Flushing, New York 11355
United StatesSite Not Available
New York-Presbyterian Hospital (NYPH)/Columbia University Irving Medical Center (CUIMC)
New York, New York 10032
United StatesActive - Recruiting
New York-Presbyterian Medical Group Queens
Flushing 5117472, New York 5128638 11355
United StatesSite Not Available
New York-Presbyterian Hospital (NYPH)/Columbia University Irving Medical Center (CUIMC)
New York 5128581, New York 5128638 10032
United StatesSite Not Available
Duke University
Durham, North Carolina 27705
United StatesActive - Recruiting
Duke University
Durham 4464368, North Carolina 4482348 27705
United StatesSite Not Available
Cleveland Clinic (Fairview)
Cleveland, Ohio 44111
United StatesSite Not Available
MetroHealth
Cleveland, Ohio 44109
United StatesActive - Recruiting
The Cleveland Clinic
Cleveland, Ohio 44111
United StatesActive - Recruiting
The Ohio State University
Columbus, Ohio 43210
United StatesActive - Recruiting
MetroHealth
Cleveland 5150529, Ohio 5165418 44109
United StatesSite Not Available
The Cleveland Clinic
Cleveland 5150529, Ohio 5165418 44111
United StatesActive - Recruiting
The Ohio State University
Columbus 4509177, Ohio 5165418 43210
United StatesSite Not Available
Medical University of South Carolina
Charleston, South Carolina 29425
United StatesActive - Recruiting
Medical University of South Carolina
Charleston 4574324, South Carolina 4597040 29425
United StatesSite Not Available
Baylor College of Medicine
Houston, Texas 77030
United StatesActive - Recruiting
UT Health Houston
Houston, Texas 77030
United StatesSite Not Available
UT Health San Antonio
San Antonio, Texas 78229
United StatesSite Not Available
Baylor College of Medicine
Houston 4699066, Texas 4736286 77030
United StatesSite Not Available
UT Health Houston
Houston 4699066, Texas 4736286 77030
United StatesSite Not Available
UT Health San Antonio
San Antonio 4726206, Texas 4736286 78229
United StatesSite Not Available
University of Utah
Salt Lake City, Utah 84132
United StatesActive - Recruiting
University of Utah
Salt Lake City 5780993, Utah 5549030 84132
United StatesSite Not Available

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