Anesthesia With Endotracheal Laser Tube

August 24, 2021 updated by: Timea Bocskai, University of Pecs

Anesthesia of Endolaryngeal Surgery With a Special Endotracheal Laser Tube

The study examines the special endotracheal laser tube during anesthesia of endolaryngeal laser surgery.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The special endotracheal tube is covered by a special aluminum tape.

Study Type

Observational

Enrollment (Actual)

30

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Hungary
      • Pecs, Hungary
        • PTE Department of ENT

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

patient with endolaryngeal laser surgery and after 18 years

Description

Inclusion Criteria:

  • laser surgery

Exclusion Criteria:

  • allergy of propofol

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
anesthesia with laser tube
The special endotracheal (ET) laser tube is tested during endolaryngeal laser surgery. Anesthesia type is the total intravenous anesthesia with propofol. We tested the application of ET laser tube in propofol anesthesia.
Other: Application of ET laser tube in propofol anesthesia
The special ET laser tube covered by aluminum tape is used during anesthesia of endolaryngeal laser surgery.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of Participants With Side Effects
Time Frame: 5 months
problem with airway or special laser tube
5 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of Pecs

Investigators

  • Study Chair: Lajos Bogar, MedHabil, PTE Department of the Anesthesiology and Intensive Therapy
  • Study Chair: Laszlo Lujber, PhD, PTE Department of ENT

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2017

Primary Completion (Actual)

June 5, 2017

Study Completion (Actual)

June 16, 2017

Study Registration Dates

First Submitted

January 29, 2017

First Submitted That Met QC Criteria

February 2, 2017

First Posted (Estimate)

February 7, 2017

Study Record Updates

Last Update Posted (Actual)

September 20, 2021

Last Update Submitted That Met QC Criteria

August 24, 2021

Last Verified

August 1, 2021

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 6419

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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