- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02943421
Transverse B-Lynch in Management of Placenta Accreta
June 26, 2018 updated by: Ahmed Mohamed Abbas, Assiut University
Evaluation of the Efficacy of Transverse B-Lynch in Management of Placenta Accreta
Placenta accreta is considered a severe pregnancy complication that may be associated with massive and potentially life-threatening intrapartum and postpartum hemorrhage.
Life-threatening bleeding is the most common complication to be associated with this condition; the average blood loss at time of delivery is reported to be 3000-5500 mL, which leads to significant postoperative morbidity and death.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Cairo
-
Assiut, Cairo, Egypt, 002
- Ahmed Abbas
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
the study encompassing women managed by conservative transverse B-Lynch during cesarean section due to placenta accreta
Description
Inclusion Criteria:
1. All pregnant women with placenta previa as diagnosed by ultrasound with suspicion of abnormal placentation by Doppler us, confirmed intraoperatively undergoing either emergent or elective cesarean
Exclusion Criteria:
- Patients who will be managed by hysterectomy
- Patients who will be managed by conservative leaving the placenta in-situ
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Estimated intraoperative blood loss
Time Frame: 30 min
|
30 min
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2016
Primary Completion (Actual)
February 3, 2018
Study Completion (Actual)
May 5, 2018
Study Registration Dates
First Submitted
October 21, 2016
First Submitted That Met QC Criteria
October 21, 2016
First Posted (Estimate)
October 24, 2016
Study Record Updates
Last Update Posted (Actual)
June 27, 2018
Last Update Submitted That Met QC Criteria
June 26, 2018
Last Verified
June 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MAP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Decrease Maternal Morbidity
-
Assiut UniversityCompletedDecrease Maternal MorbidityEgypt
-
Assiut UniversityCompleted
-
Northwell HealthNational Institute of Nursing Research (NINR)Not yet recruiting
-
Hospital Civil de GuadalajaraActive, not recruitingMaternal-Fetal Relations | Anesthesia | Perinatal MorbidityMexico
-
Amit ArjyalBagmati Rural Municipality, Lalitpur, Nepal; Konjyosom Rural Municipality,... and other collaboratorsNot yet recruitingMaternal Health | Infant Health | Severe Maternal Morbidity | Institutional Delivery | Birth Preparedness and Complication Readiness | Neonatal Adverse OutcomeNepal
-
Assistance Publique - Hôpitaux de ParisCompletedMaternal Morbidity | Obstetrics | Gynecology | QualityFrance
-
University of OttawaJimma University; Ethiopian Ministry of Health, Jimma ZoneCompletedMaternal Mortality | Maternal Morbidity
-
Michigan State UniversitySpectrum Health Hospitals; Hurley MIHP and Healthy Start; Ascension MIHP and... and other collaboratorsEnrolling by invitationHealth Disparities | Maternal Morbidity and MortalityUnited States
-
Harvard School of Public Health (HSPH)Brigham and Women's Hospital; Bill and Melinda Gates Foundation; World Health... and other collaboratorsCompletedMaternal Death | Stillbirth | Maternal Morbidity | Neonatal DeathIndia
-
Emory UniversityNational Institute on Minority Health and Health Disparities (NIMHD)Active, not recruitingMaternal Death | Maternal MorbidityUnited States
Clinical Trials on Transverse B-Lynch suture
-
Aswan University HospitalUnknownCesarean Section ComplicationsEgypt
-
IRCCS Azienda Ospedaliero-Universitaria di BolognaCompleted
-
Ain Shams Maternity HospitalCompletedBleeding in Cesarean SectionEgypt
-
Dongyu WangFirst Affiliated Hospital, Sun Yat-Sen University; The Third Affiliated Hospital... and other collaboratorsCompleted
-
Cairo UniversityUnknown
-
Northern Jiangsu People's HospitalCompletedIleostomy | Ileostomies | Loop IleostomiesChina
-
The Catholic University of KoreaCompletedType 2 Diabetes | Cardiac Autonomic NeuropathyKorea, Republic of
-
Regeneron PharmaceuticalsActive, not recruiting