Status:

TERMINATED

Impact of a Intra-tracheal Intubation With Curarization or Without Curarization

Lead Sponsor:

Nantes University Hospital

Conditions:

Intubation Complication

Eligibility:

All Genders

18+ years

Brief Summary

VHIntubation is a French monocentric and observational study that will assess the impact of two intra-tracheal intubation preparation procedures (curarization versus remifentanil) on the voice, using ...

Detailed Description

Some surgeries are known to expose patients to voice disorders (thyroidectomy, parathyroidectomy, carotid surgery…). However, voice disorders can be due, among other things, to a laryngeal nerves alte...

Eligibility Criteria

Inclusion

  • Patients included in " REMICRUSH " study
  • patient's non-opposition to participation in research
  • Inclusions criteria in REMICRUSH are :
  • male or female aged from 18 to 80 years old
  • surgery requiring general anaesthesia with tracheal with oro-tracheal intubation
  • Rapid sequence intubation indication
  • aspiration risk defined as : fasting \< 6h00, digestive occlusion, functional ileus, vomiting \< 12h00, orthopaedic trauma \< 12h00, severe gastric reflux, gastroparesis and/or dysautonomia and or gastro-oesophagus surgery
  • signed informed consent sheet ; or emergency procedure if impossible

Exclusion

  • Patients non-included in " REMICRUSH " study
  • Patients with cervical surgery
  • Patient declines to participate in research
  • Exclusion criteria in REMICRUSH are :
  • planned impossible intubation
  • suspected/known allergy to neuromuscular blockade or remifentanil
  • neuromuscular disease forbidding neuromuscular blockade use
  • Prolonged neuromuscular block former episode
  • Malignant hyperthermia former episode
  • Pre-operative respiratory failure (spO2\< 95%)
  • Pre-operative hemodynamic failure (use of vasopressor) cardiac arrest
  • A woman of childbearing age who has an active pregnancy and/or clinical signs suggestive of an active pregnancy and/or does not have a contraceptive or contraceptive method and has had unprotected sex within 15 days of the last menstrual period.
  • Patients under justice protection
  • Use of etomidate for anesthetic induction

Key Trial Info

Start Date :

June 16 2020

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

December 31 2020

Estimated Enrollment :

7 Patients enrolled

Trial Details

Trial ID

NCT04364633

Start Date

June 16 2020

End Date

December 31 2020

Last Update

April 19 2022

Active Locations (1)

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1

Nantes University Hospital

Nantes, France, 44093