ClinicalTrials.Veeva

Menu

Do Throat Pack Used in Dental Treatments Under General Anesthesia of Patients Have an Effect on PONV and Sore Throat?

Ç

Çukurova University

Status

Not yet enrolling

Conditions

Dental Caries
Postoperative Nausea and Vomiting
Sore-throat

Treatments

Procedure: throat pack

Study type

Interventional

Funder types

Other

Identifiers

NCT06169306
CUDHF-PABD

Details and patient eligibility

About

The aim of this study is to investigate the effect of throat packs on PONV in dental treatments under general anesthesia in special health care needs.

Full description

Throat packs are widely used to prevent aspiration of blood and other debris, especially in orofacial surgeries and dental treatments performed under general anesthesia. Aspiration of blood and other secretions into the stomach is one of the important causes of PONV. There is not much evidence that throat packs prevent nausea and vomiting after surgery. The most critical side effects of throat pack application are sore throat, difficulty swallowing, and being forgotten before extubation.

The incidence of cavities and other dental problems is higher in special health care needs due to reasons such as inadequate oral hygiene, malocclusion, high-carbohydrate diet, and lack of awareness about dental health. In this group of patients, dental treatments are primarily performed under general anesthesia. Since side effects are more difficult to identify by the patient, the procedures, technical applications and anaesthesia methods should be those with the least potential for side effects. Evidence is needed regarding the effect of throat packing on PONV. In this study, researchers planned to investigate the effects of using throat tampons during dental treatments under general anesthesia on PONV and sore throat in participants requiring special health care.

Enrollment

74 estimated patients

Sex

All

Ages

5 to 16 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Volunteering to participate in the study with parental consent
  • Being between the ages of 5-16
  • Being grade 1 or 2 according to the ASA (American Society of Anesthesiologists) classification
  • At least one primary or permanent and one restorative. Having undergone treatment (amalgam or composite restoration)

Exclusion criteria

  • Having a tracheostomy
  • Being evaluated as having difficult intubation
  • Having an additional disease related to the oesophagus, stomach or intestines, having a percutaneous endoscopic gastrostomy,
  • Having a history of PONV,
  • Having morbid obesity,
  • Having high airway pressure,
  • Having a history of allergy to the drugs to be used,
  • Needing an anaesthetic agent other than the anaesthesia method to be applied
  • Having advanced mental retardation that prevents data collection

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

74 participants in 2 patient groups

control
No Intervention group
Description:
Following endotracheal intubation, no throath pack will inserted into the hypopharynx.
throath pack
Experimental group
Description:
Following endotracheal intubation, throath pack will inserted into the hypopharynx.
Treatment:
Procedure: throat pack

Trial contacts and locations

0

Loading...

Central trial contact

Hacer N Uğuz; Sibel Tetiker, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems