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NCT03044418 Clinical Trial

Anesthesia With Endotracheal Laser Tube

Anesthesia Clinical Trial

Official title:
Anesthesia of Endolaryngeal Surgery With a Special Endotracheal Laser Tube

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03044418
Other study ID # 6419
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2017
Est. completion date June 16, 2017

Study information
Verified date August 2021
Source University of Pecs
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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

Description:

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

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date June 16, 2017
Est. primary completion date June 5, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - laser surgery Exclusion Criteria: - allergy of propofol

Study Design

Related Conditions & MeSH terms

Intervention

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.

Locations
Country Name City State
Hungary PTE Department of ENT Pecs

Sponsors (1)
Lead Sponsor Collaborator
University of Pecs

Country where clinical trial is conducted

Hungary, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of Participants With Side Effects problem with airway or special laser tube 5 months
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