Investigation of hypo gastric arterial ligation in placenta accreta disorders

Not Applicable

Recruiting

• Conditions: Placenta adherent disorder.; Third-stage hemorrhage; O72.0

• Registration Number: IRCT20190123042467N1
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 26 August 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 70

Inclusion Criteria

?Diagnosis of placenta accreta disease by two experienced gynecologists by Color Doppler Ultrasonography
Awareness of the patient and her/his family from the study and signing the consent form

Exclusion Criteria

Patient's dissatisfaction for participating in the study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Amount of blood loss during operation. Timepoint: Immediately after intervention. Method of measurement: The amount of blood inside the aspirator.;Frequency of deep vein thrombosis. Timepoint: Seven days after operation. Method of measurement: Duplex ultrasonography.;Amount of used blood products during operation. Timepoint: End of operation. Method of measurement: Direct counting.;Operation time. Timepoint: End of operation. Method of measurement: Timer.;Time of hospitalization. Timepoint: Seven days after operation. Method of measurement: Investigation of medical record.