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Assessment of Post-operative Sore Throat After Scheduled General Anesthesia

Assessment of Post-operative Sore Throat After Scheduled General Anesthesia

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04115865
Acronym
POST
Enrollment
0
Registered
2019-10-04
Start date
2020-01-31
Completion date
2021-01-31
Last updated
2020-03-27

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

Conditions

Intubation;Difficult, Sore Throat

Brief 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

Interventions

DEVICEEndotracheal sonde or laryngeal mask

Healthy subjects ; requiring general anesthesia with endotracheal or endobuccal device

Sponsors

University Hospital, Lille
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Incidence of sore throatWithin 24 hours of surgery

Secondary

MeasureTime frameDescription
Severity of sore throat,At exit of the post-interventional monitoring room, at 24 hours of surgery or exit of hospital
type of sore throat risk factorAt exit of the post-interventional monitoring room, at 24 hours of surgery or exit of hospital(technique of intubation, analgesic treatment for surgery…)

Outcome results

None listed

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