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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05806528
Other study ID # Soh-Med-23-03-03MS
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date April 1, 2023
Est. completion date March 1, 2024

Study information

Verified date March 2023
Source Sohag University
Contact Mariam s Mahmoud, Resident
Phone 01061816280
Email mariamsabri20@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will be conducted on women who have a diagnosis of placenta previ and using ultrasound to make the placenta invasion index and compare the accuracy of the diagnosis during the caesarean section whether it is accreta or not with determining the site and depth of invasion


Description:

This study will be conducted on women who have a diagnosis of placenta previ and using ultrasound to make the placenta invasion index and compare the accuracy of the diagnosis during the caesarean section whether it is accreta or not with determining the site and depth of invasion and whether there is injury occurred in the urinary system and Determining the amount of blood transfusion and admission of intensive care, or whether the patient death


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date March 1, 2024
Est. primary completion date January 1, 2024
Accepts healthy volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - all placenta previa and low laying placenta will be included Exclusion Criteria: - patient with sever attack

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Ultrasound
Use ultrasound to make placental invasion index

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sohag University

Outcome

Type Measure Description Time frame Safety issue
Primary Role of placental invasion index in decision making of placenta accreta Use of ultrasound to make placenta invasion index and compare it intraoperative 1 year
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