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Preventive EXACYL® on Perioperative Bleeding During Orthognathism of Maxillary Surgery — LEFORTEXACYL  

Surgery Clinical Trial

Official title:
Preventive EXACYL® on Perioperative Bleeding During Orthognathism of Maxillary Surgery

Clinical Trial Summary

Prospective, randomized, double-blind, placebo-controlled, mono center, Phase III trial to compare EXACYL in preventive with placebo on perioperatory bleeding in orthognathism surgery.

Clinical Trial Description

The aim of our study was to evaluate the clinical value of preventive treatment EXACYL® on bleeding during surgery to orthognathism. Our hypothesis is that this preventive treatment is not enough reduces bleeding to cause a change in patient management (count additional blood count, extra padding, transfusion). Prospective equivalence trial type controlled by two parallel group, randomized, triple-blind (patient, surgical team, anesthesia team). - EXACYL® Group: 1 syringe 1g EXACYL® on one hour + 1 syringe 1g EXACYL® on 8 hours - Control group: 1 syringe 30 mL of saline on one hour + 1 syringe 30 mL saline on 8 hours Main criteria is amount of blood during the entire hospitalization: bleeding during surgery completed in the amount of blood present in the suction drains and nasogastric tube until ablation thereof. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02702128
Study type Interventional
Source University Hospital, Lille
Contact
Status Completed
Phase Phase 3
Start date January 3, 2016
Completion date June 30, 2018
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