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The Effect of Preoperative Chewing Gum on Anxiety and Sore Throat in Patients With Laryngeal Mask Airway

A

Ankara Medipol University

Status

Invitation-only

Conditions

Throat Pain
Laryngeal Mask
Anxiety

Treatments

Other: Chewing Gum

Study type

Interventional

Funder types

Other

Identifiers

NCT06168981
2023/197

Details and patient eligibility

About

This study was planned to investigate the effect of chewing gum in the preoperative period on patients' sore throat and anxiety levels.

Full description

Postoperative sore throat is a common complaint (1,2). It is reported in the literature that there are various pharmacological methods to reduce this condition, such as the use of nebula, corticosteroids, nonsteroidal anti-inflammatory drugs, or lidocaine. However, these methods have various advantages and disadvantages (3,4). Chewing gum, one of the non-pharmacological methods may be safer for the patient. Chewing gum increases salivary gland secretion and provides lubrication of the oral cavity (5). For this reason, it was thought that chewing gum before surgery could reduce throat pain after using a laryngeal mask due to the effect it provides. It has been determined that there are few experimental studies on the subject in the literature (6,7).

The presence of preoperative anxiety may lead to an increase in the need for intraoperative anesthesia and analgesic consumption in the postoperative period (8,9). However, it may cause a decrease in patient satisfaction and prolong the recovery process in the postoperative period (8,9). Pharmacological approaches can be applied to address this concern. However, non-pharmacological approaches may be safer for patients. Chewing gum during this process can also reduce patients' anxiety levels. A sufficient number of studies on the subject could not be found (10).

The study will conduct as a prospective randomized controlled trial. After obtaining verbal and written consent from the patients before and after the surgery, the study will conduct with various data collection forms.

These forms are; patient Identification form, Amsterdam Preoperative Anxiety and Information Scale (APAIS), Visual Analogue Scale (VAS). Patients will randomize. The chewing gum group in group- I (n=46), and group II (n=46) will be the control group. We have two stage.In first stage; anxiety levels will be measured for both group. In second stage; throat pain will evaluated at 2.-4.-6. hours.

Enrollment

92 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Undergoing elective surgery
  • Being intubated with a laryngeal mask
  • Being ASA (American Society of Anesthesiologists) I-II

Exclusion criteria

  • Using cigarette

    • Having asthma
    • Having chronic laryngitis
    • Having gastroesophageal reflux
    • Steroid use in the preoperative or intraoperative period
    • Mallampati score greater than two

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

92 participants in 2 patient groups

Chewing Gum
Experimental group
Description:
Before the surgery, the patient will chew gum for 2 minutes and routine nursing care will be applied. Anxiety level will be evaluated before and after chewing gum.
Treatment:
Other: Chewing Gum
Control Group
No Intervention group
Description:
Anxiety level will be evaluated before and after routine nursing care.

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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