EUCTR2016-002197-13-ES
Active, not recruiting
Phase 1
IMPLICATION OF TWO ANESTHETIC TECHNIQUES: SEVOFLURANE VERSUS PROPOFOL TO REDUCE BLOOD LOSS IN ORTHOGNATHIC SURGERY
Servicio de Anestesiología y Reanimación0 sitesOctober 26, 2016
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Servicio de Anestesiología y Reanimación
- Status
- Active, not recruiting
- Last Updated
- 9 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients \= 18 and \= 65 years old.
- •Classification ASA (American Society of Anesthesiologists) I or II.
- •orthognathic surgery scheduled bimaxillary
- •Signed informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range 100
- •F.1\.3 Elderly (\>\=65 years) no
- •F.1\.3\.1 Number of subjects for this age range
Exclusion Criteria
- •Patients who do not wish to consent to participate in the study.
- •Hemodynamic instability determined by the need for continuous infusion of inotropic or vasopressor.
- •Severe heart disease (Grades III and IV, NYHA)
- •Kidney disease (creatinine clearance \= 30 mL / min)
- •Liver disease (Grade C Child\-Pugh).
- •Diabetes Mellitus Type I or II compensated or decompensated.
- •Previous surgery in the surgical field including orthognathic surgery.
- •Patients with treatments or diseases affecting the coagulation cascade or platelet aggregation.
Outcomes
Primary Outcomes
Not specified
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