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Clinical Trial Summary

Patient undergoing surgery is exposed to many stressors: diachronic (gesture anticipation), synchronic (intraoperative aggression) and historical (subject's personality). Reducing the level of stress experienced is a factor for improving the quality of the surgical gesture and the simplicity of the follow-up. The previous methods used were intended to reduce the body's reactivity to aggressions through anaesthesia consultation and L-Tyrosine supplementation. Currently with the progression of outpatient surgery and the need for early rehabilitation, L-Tyrosine supplementation is suppressed to improve recovery. Some patients, however, have a high level of stress that may require anxiolysis when the ideal treatment does not exist (ineffective hydroxyzine, benzodiazepines having many side effects). The strategy of this work is to improve the body's ability to respond to stressors, by administering l-tyrosine with no impact on waking or returning home.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05782829
Study type Interventional
Source Centre Hospitalier Universitaire de Nice
Contact Isabelle ROUQUETTE-VINCENTI, MD, PhD
Phone +377 97 98 98 19
Email isabelle.rouquette-vincenti@chpg.mc
Status Not yet recruiting
Phase N/A
Start date April 2023
Completion date April 2024

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