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Assessment of Hematologic Parameters Before and After Bimaxillary Orthognathic Surgery

Surgical Blood Loss Clinical Trial

Official title:
Assessment of Changes of Hematological Parameters and Need for Blood Transfusion in Bimaxillary Orthognathic Surgery

Clinical Trial Summary

The purpose of the present study was to compare some hematologic parameters and operation time in patients who underwent esthetic bimaxillary surgery under hypotensive anesthesia.

Clinical Trial Description

Patients who underwent bimaxillary surgery were prospectively evaluated. Patients were divided into groups based on the surgical procedure and sex (predictor variables). Hemoglobin, red blood cells, hematocrit, and platelet were the primary outcome variables, operation time was the secondary outcome variable, and the patients' age and weight were the other variables. ;

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02364765
Study type Interventional
Source Federal University of Minas Gerais
Contact
Status Completed
Phase N/A
Start date August 2010
Completion date June 2012
View Details
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