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Clinical Trials/NCT06412627
NCT06412627
Not yet recruiting
Not Applicable

The Effect of Intervention About Dry Mouth and Thirst in Patients With Endotracheal Tube

Changhua Christian Hospital1 site in 1 country100 target enrollmentMay 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endotracheal Tube
Sponsor
Changhua Christian Hospital
Enrollment
100
Locations
1
Primary Endpoint
Oral moisture checking device
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

This is an experimental study aimed at exploring the effectiveness of using 4°C frozen gauze with normal saline for relieving dry mouth and thirst in patients with endotracheal tubes.

Detailed Description

Long-term placement of endotracheal tubes often causes discomfort, including lip ulcers, laryngeal pain, and dry oral mucosa, leading to frequent complaints of dry mouth and thirst among conscious patients. However, these symptoms are commonly overlooked in the nursing process, resulting in emotional distress and irritability in patients. Although healthcare providers recognize the issue of dry mouth and thirst in patients with endotracheal tubes, effective management is challenging due to concerns about treatment limitations, aspiration pneumonia, and the risk of coughing or vomiting. This experimental study aims to explore the effectiveness of using 4°C frozen gauze soaked in normal saline to relieve dry mouth and thirst in patients with endotracheal tubes.

Registry
clinicaltrials.gov
Start Date
May 2024
End Date
January 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Endotracheal intubation.
  • Aged 18 years or older.
  • Patient or family members are willing to sign the consent form.

Exclusion Criteria

  • History of head and neck cancer.
  • Oral mucosal damage, swelling, or bleeding that precludes placement of a moist gauze pad.

Outcomes

Primary Outcomes

Oral moisture checking device

Time Frame: Change from baseline dry mouth at Day 3, and Day 7

The oral moisture checking device was utilized to assess symptoms of dry mouth in participants. This study utilized an oral moisture checking device produced by Life Co., Ltd. of Japan, which measures the moisture content within the oral cavity using the principle of bioelectrical impedance analysis (BIA). The measurement method involves placing a specialized plastic sleeve over the tongue approximately one centimeter from the tip and applying a force of 200 grams. A measurement is obtained after about 2 seconds. A reading below 27.9 indicates dryness, a reading between 28 and 29.5 is considered borderline, and readings of 29.6 and above are normal. Both the sensitivity and specificity of this method are 0.8.

Secondary Outcomes

  • Bedside oral examination scale(Change from baseline oral health function at Day 3, and Day 7)
  • Oral health assessment Tool(Change from baseline oral health status at Day 3, and Day 7)

Study Sites (1)

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