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Does the Use of a Videolaryngoscope Modifies Anesthetic Induction ?

Does the Use of a Videolaryngoscope Modifies Anesthetic Induction ?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02245789
Acronym
MGM-PicRemi
Enrollment
50
Registered
2014-09-22
Start date
2014-09-30
Completion date
2015-02-28
Last updated
2016-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tracheal Intubation

Brief summary

Videolaryngoscopes become widely used. The aim of this study is to compare anesthetic induction when patients are tracheally intubated using a MacGraph Mac videolaryngoscope or a conventional MacIntosh laryngoscope. Tracheal intubation induces a nociceptive stimulation. Hypothesis is that the use of a videolaryngoscope induces a less pronounced nociceptive stimulation and, consequently, that it modifies the anesthetic drugs requirement. .

Detailed description

All patients will received a standardized anesthetic procedure : combined closed-loop anesthesia system using bispectral index as control variable and two proportional-differential control algorithms, a propofol and a remifentanil target-controlled infusion system. The effectiveness of such a closed-loop anesthesia system has been demonstrated in a prospective, randomized study. Patients will be randomized in two groups : intubation using a conventional MacIntosh laryngoscope or intubation using a videolaryngoscope. If our hypothesis is confirmed, the required concentration of remifentanil, an opioid agent, will be reduced in the group using a videolaryngoscope.

Interventions

PROCEDURETracheal intubation

Tracheal intubation will be performed using a Macintosh laryngoscope or a McGrath Mac videolaryngoscope

DRUGPropofol and remifentanil anesthesia

The standardized anesthetic procedure used a closed-loop anesthesia system with bispectral index as control variable and with two proportional-differential control algorithms, one for propofol target-controlled infusion system and one for remifentanil target-controlled infusion system.

Sponsors

Hopital Foch
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* patient scheduled for a general anesthesia with orotracheal intubation

Exclusion criteria

* predictable risk of difficult mask ventilation or of difficult tracheal intubation * necessity of a rapid sequence induction * contra-indication to the use of the automated administration of propofol and of remifentanil * contra-indication to the use of atracurium * Otolaryngology, thoracic surgery, or intracranial surgery

Design outcomes

Primary

MeasureTime frameDescription
Required dose of opioid to counteract nociceptive stimulation1 hourTracheal intubation induces a nociceptive stimulation. Hypothesis is that the use of a videolaryngoscope induces a less pronounced nociceptive stimulation and, consequently, that the required maximal concentration of remifentanil is lower than when a standard laryngoscope is used.

Secondary

MeasureTime frameDescription
Characteristics of tracheal intubationone hourtime to obtain the first capnogram
Characteristics of anesthesiaone hourPeak concentration of propofol
Complications of intubationone dayThroat pain and hoarseness
Ergonomic evaluation of the deviceone hourquestionnaire Qusi

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026