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NCT04115865 Clinical Trial

Assessment of Post-operative Sore Throat After Scheduled General Anesthesia

Sore Throat Clinical Trial

— POST  

Official title:
Assessment of Post-operative Sore Throat After Scheduled General Anesthesia

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT04115865
Other study ID # 2018_96
Secondary ID 2019-A02077-50
Status Withdrawn
Phase
First received
Last updated
Start date January 2020
Est. completion date January 2021

Study information
Verified date March 2020
Source University Hospital, Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Precise description of the technique for intubation or laryngeal mask placement during general anesthesia Research on factors that can influence sore throat due to the placement of an endobuccal or endotracheal device during general anesthesia

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date January 2021
Est. primary completion date January 2020
Accepts healthy volunteers No
Gender All
Age group 6 Years and older
Eligibility Inclusion Criteria:

- General Anesthesia required Endotracheal or endobuccal device

Exclusion Criteria:

- Tracheotomy per or post surgery

- Patient with pre-operative pharyngeal irritation.

- Patient with a prior respiratory tract infection.

- Surgery of the laryngeal or tracheal vein, old or new

- Surgery scheduled less than 24 hours ago.

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Endotracheal sonde or laryngeal mask
Healthy subjects ; requiring general anesthesia with endotracheal or endobuccal device

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Lille

Outcome
Type Measure Description Time frame Safety issue
Primary Incidence of sore throat Within 24 hours of surgery
Secondary Severity of sore throat, At exit of the post-interventional monitoring room, at 24 hours of surgery or exit of hospital
Secondary type of sore throat risk factor (technique of intubation, analgesic treatment for surgery…) At exit of the post-interventional monitoring room, at 24 hours of surgery or exit of hospital
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