Intratracheal Intubation
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients over 18 years of age; men or women; who had undergone total or partial thyroidectomy; Classification of ASA grade I or II; who agreed to sign the free and informed consent
Exclusion criteria
Exclusion criteria: Patients who refused to participate in the study; patients with difficult orotracheal intubation (OTI) (trachea not intubated on the first attempt); smoking patients; cuff rupture during OTI; patients with cardiac, pulmonary, or neuropathies; patients with previous laryngeal and/or tracheal surgeries, with risk of aspiration of gastric contents, and with the need to use a nasogastric tube were excluded
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: It is expected to observe a lower physiological reflex during extubation, shorter time to wake up and recover from speech, as well as lower perioperative pressure levels in the lidocaine group.;Found outcome 1: There was no protective effect of the use of physiological reflex damage during extubation, time to wake up and speech recovery, on perioperative pressure levels in the lidocaine group. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 2: Observe protective effect on swallowing sensation, Ability to sustain phonation and sustain adequate volume and complaints, dysphonia, emesis, vocal fatigue, hemoptysis, airway inflammation, fullness, hoarseness, foreign body sensation, whisper, cough, fullness , hoarseness and foreign body sensation in the lidocaine group.;Found outcome 2: There was no protective effect on the sensation of swallowing, Ability to sustain phonation and sustain adequate volume and complaints, dysphonia, emesis, vocal fatigue, hemoptysis, airway inflammation, fullness, hoarseness, foreign body sensation, whisper, cough , fullness, hoarseness and foreign body sensation in the lidocaine group. | — |
Countries
Brazil
Contacts
Hospital São Domingos