- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03044418
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
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Pecs, Hungary
- PTE Department of ENT
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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.
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The special ET laser tube covered by aluminum tape is used during anesthesia of endolaryngeal laser surgery.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of Participants With Side Effects
Time Frame: 5 months
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problem with airway or special laser tube
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5 months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
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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