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Completed

NCT Number: NCT02575716

Comparison of Intubating Condition of the Mcgrath Videolaryngoscope With and Without Muscle Relaxant

The objective of this study was to evaluate intubating condition using the McGrath® VL Series 5, with and without muscle relaxant

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Department of anesthesiology

Hat Yai, Changwat Songkhla, 90110, Thailand

About this study

Thirty-four patients with ASA classification I-II, who required oroendotracheal tube intubation, were studied in this prospective, double-blinded, randomized, clinical trial. Anesthesia was induced using fentanyl 1.5 mcg/kg, xylocaine 1.5 mg/kg and propofol 3 mg/kg. Patients were randomly assigned to one of the two groups to receive either rocuronium 0.6 mg/kg or saline intravenously. The Mcgrath® VL intubation was initiated after 90s, when the patients were fully relaxed. The primary outcome was to compare tracheal intubating conditions between two groups. The secondary outcomes were the success rate in the first attempt intubation, time to intubation, the required propofol dose for intubation and anesthetic complications. Statistical analyses were performed using the R program version 2.14.2. The level of statistical significance was set at p < 0.05.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-65 years old.
  • ASA class I-II.
  • Elective surgery required general anesthesia with oroendotracheal intubation

Exclusion criteria

  • Suspected or known difficult airway.
  • Patient with risk of aspiration with required of rapid sequence induction .
  • Plan remained intubation.
  • Allergic to drugs used in the study.
  • Renal or hepatic disease.

Treatment and study plan

Videolaryngoscope

Device

Intubation with McGrath video laryngoscope after muscle relaxant

Primary outcomes

  1. Intubating condition.

    Time frame: one year

    number of participants with 34 people

Secondary outcomes

  1. Success rate in the first attempt intubation.

    Time frame: one year

  2. Time to intubation

    Time frame: One year

  3. The required propofol dose for intubation without muscle relaxant.

    Time frame: one year

  4. Events during the intubation attempts occurred.

    Time frame: one year

Sponsors and collaborators

Lead sponsor

Prince of Songkla University

Other

Registry information

Important dates

Study start
2013
Primary completion
2013
Study completion
2014
First posted
Oct 15, 2015
Registry last updated
Oct 15, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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