Clinical Trials Directory

Trials / Completed

CompletedNCT02364765

Assessment of Hematologic Parameters Before and After Bimaxillary Orthognathic Surgery

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
53 (actual)
Sponsor
Federal University of Minas Gerais · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGRemifentanilElective bimaxillary orthognathic surgery consisting of a unsegmented LeFort I osteotomy combined with a bilateral sagittal split osteotomy, under the influence of mean remifentanil administration of 0.3 mg/kg/hour

Timeline

Start date
2010-08-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2015-02-18
Last updated
2015-02-18

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT02364765. Inclusion in this directory is not an endorsement.