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Multidisciplinary Team in Management of Placenta Accreta

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ClinicalTrials.gov Identifier: NCT03372538
Recruitment Status : Not yet recruiting
First Posted : December 13, 2017
Last Update Posted : December 13, 2017
Sponsor:
Information provided by (Responsible Party):
sarah mohamed hassan, Kasr El Aini Hospital

Brief Summary:
comparative study between the incidence of urological injury in case of placenta accreta in cases where urological surgical staff are participating in the operation from the start and in cases where the operation is carried by the gynecological staff only

Condition or disease Intervention/treatment
Placenta Accreta Procedure: cesarean section or cesarean hysterectomy

Detailed Description:
cohort of 1000 patients of placenta accreta are followed regarding the incidence of urological injury in the cases with assistance from the urological staff members

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Study Type : Observational
Estimated Enrollment : 1000 participants
Observational Model: Case-Control
Time Perspective: Prospective
Official Title: is There Any Superior Benefit of Multidisciplinary Team in Management of Placenta Accreta
Estimated Study Start Date : December 2017
Estimated Primary Completion Date : March 2018
Estimated Study Completion Date : March 2018

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Cesarean Section

Group/Cohort Intervention/treatment
multidisciplinary team group
500 patients of placenta accreta managed by obstetricans and urologists
Procedure: cesarean section or cesarean hysterectomy
upper segment cesarean section and or cesarean hysteroctomy

obstetricians only group
500 patients of placenta accreta managed by obstetricans only
Procedure: cesarean section or cesarean hysterectomy
upper segment cesarean section and or cesarean hysteroctomy




Primary Outcome Measures :
  1. urological injury [ Time Frame: intraoperative ]
    badder or ureteric injury



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Ages Eligible for Study:   20 Years to 40 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
1000 patients pregnant 38 weeks with placenta accreta
Criteria

Inclusion Criteria:

  • pregnant 38 weeks
  • placenta accreta

Exclusion Criteria:

  • medical disorders complicating pregnancy

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03372538


Locations
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Egypt
Kasr El Ainiy Hospital
Cairo, Egypt, 11562
Sponsors and Collaborators
Kasr El Aini Hospital

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Responsible Party: sarah mohamed hassan, lecturer of obstetrics and gynecology, Kasr El Aini Hospital
ClinicalTrials.gov Identifier: NCT03372538     History of Changes
Other Study ID Numbers: 494608
First Posted: December 13, 2017    Key Record Dates
Last Update Posted: December 13, 2017
Last Verified: December 2017

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by sarah mohamed hassan, Kasr El Aini Hospital:
placenta accreta
Additional relevant MeSH terms:
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Placenta Accreta
Obstetric Labor Complications
Pregnancy Complications
Placenta Diseases