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Post-operative Sore Throat and Gum Chewing

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Completed

Conditions

Surgery
Anesthesia

Treatments

Other: Gum
Other: Control

Study type

Interventional

Funder types

Other

Identifiers

NCT04859101
ANES-2021-29683

Details and patient eligibility

About

The purpose of this study is to determine if chewing gum immediately prior to transport to the operating room reduces the severity of post-operative sore throat in patients who have an LMA (laryngeal mask airway) placed for procedures with duration greater than 1 hour.

Full description

Patients will be randomized into two groups. Group 1 will receive a piece of gum immediately prior to transport to the operating room. They will be asked to chew the gum for 2 minutes and then spit the gum in the garbage. Group 2 will not receive any gum. They will be asked to swallow twice and have no other intervention.

Enrollment

86 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Outpatient ambulatory surgery
  • General anesthesia utilizing a laryngeal mask airway
  • Greater than 1 hour duration

Exclusion criteria

  • Chronic laryngitis
  • Chronic bronchitis
  • Asthma
  • Gastroesophageal reflux disease
  • Smoking within the last week
  • Non-English speaking

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

86 participants in 2 patient groups

Gum
Experimental group
Description:
Group 1 will receive gum immediately prior to transport to the operating room. They will be asked to chew the gum for 2 minutes and then spit the gum in the garbage.
Treatment:
Other: Gum
Control
Other group
Description:
Group 2 will not receive any gum. They will be asked to swallow twice and have no other intervention.
Treatment:
Other: Control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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