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Use of McGrath Videolaryngoscope to Assist Transesophageal Echocardiography Probe Insertion in Intubated Patients

Use of McGrath Videolaryngoscope to Assist Transesophageal Echocardiography Probe Insertion in Intubated Patients: A Prospective Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02634047
Enrollment
80
Registered
2015-12-17
Start date
2015-09-30
Completion date
2015-11-30
Last updated
2015-12-17

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

Conditions

Other Complications of Surgical and Medical Procedures

Keywords

transesophageal echocardiography, videolaryngoscope, oropharyngeal injury

Brief summary

The primary aim of this study is to investigate the difference in the first attempt and overall success rate of different techniques for insertion of transesophageal echocardiography. Secondary aim is to investigate the difference of the duration of insertion using the selected technique, complications during insertion such as oropharyngeal mucosal injury and hematoma.

Detailed description

Eighty adult patients, who received general anaesthesia for elective open heart surgeries that required transesophageal echocardiography insertion, will be randomized by means of a computer-generated randomization order into two groups: Conventional group (Group C), and videolaryngoscope group (group VL). Success rate of the selected technique (first attempt and overall), duration of insertion for selected technique, complications such as oropharyngeal mucosal injury and hematoma will be noted.

Interventions

transesophageal echocardiography probe was inserted using a traditional blind insertion technique.

transesophageal echocardiography probe was advanced into esophagus under direct vision using videolaryngoscope

Sponsors

Antalya Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients who received general anaesthesia for open heart surgeries that required transesophageal echocardiography probe insertion

Exclusion criteria

* patients younger than 18 years and older than 70 years * oropharengeal infection * esophageal injury and anatomic abnormalities * known or predicted difficult airway

Design outcomes

Primary

MeasureTime frameDescription
difference in the first attempt and overall success rateparticipants will be followed from the beginning of the transesophageal echocardiography probe insertion through the mouth to the confirmation of successful insertion (10 minutes)investigate the difference in the first attempt and overall success rate (with percentage) of different techniques for insertion of transesophageal echocardiography probe.

Secondary

MeasureTime frameDescription
difference of the duration of insertion and complications during insertionparticipants will be followed for the duration of intraoperative period and postoperative 8 hours.investigate the difference of the duration of insertion (in seconds) using the selected technique and complications (with number and percentage) during insertion such as oropharyngeal mucosal injury and hematoma.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026