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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03372538
Other study ID # 494608
Secondary ID
Status Not yet recruiting
Phase N/A
First received December 9, 2017
Last updated December 9, 2017
Start date December 2017
Est. completion date March 2018

Study information

Verified date December 2017
Source Kasr El Aini Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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


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


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 1000
Est. completion date March 2018
Est. primary completion date March 2018
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- pregnant 38 weeks

- placenta accreta

Exclusion Criteria:

- medical disorders complicating pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
cesarean section or cesarean hysterectomy
upper segment cesarean section and or cesarean hysteroctomy

Locations

Country Name City State
Egypt Kasr El Ainiy Hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Kasr El Aini Hospital

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary urological injury badder or ureteric injury intraoperative
See also
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