Study to Compare the Effect of Two Different Types of Humidifier on the Endotracheal Tube Patency

Cancer of Head and Neck Clinical Trial

Official title:

Study to Compare the Effect of Two Different Types of Humidifier on the Endotracheal Tube Patency

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02780765
• Other study ID #: 1665
• Status: Completed
• Phase: N/A
• Start date: July 2016
• Est. completion date: January 2017

Study information

• Verified date: August 2018
• Source: Tata Memorial Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

60 post operative patients who are kept intubated overnight & are spontaneously breathing will be either supplied humidified oxygen Heated Humidifier(HH) or conventional mist nebulizer.

Temperature of inspired gas at the Y piece will be measured.

Sterile water will be used for HH & Mist nebuliser.

The suctioning of endotracheal tube (ETT) will be done once every 2 hourly by nurse/ doctor/trained personnel and additional suctioning if required.

Description:

60 post operative patients who are kept intubated overnight & are spontaneously breathing will be selected in Tata Memorial Hospital (TMH), Mumbai. 30 patients will be supplied through humidified oxygen using FISHER & PAYKEL MR 370 Heated Humidifier(HH) & 30 patients through conventional mist nebulizer.

Temperature of inspired gas at the Y piece will be measured as surrogate marker for quality of humidification. Continuous monitoring of temperature will be done using standard monitor.

The reusable HH will be subjected to disinfection between patients. Sterile water will be used for HH & Mist nebuliser.

The suctioning of endotracheal tube (ETT) will be done once every 2 hourly by nurse/ doctor/trained personnel.

Based on patient's clinical condition , additional suctioning will be done. Frequency of additional suctioning , reason for suctioning will be noted.

Information regarding the age, sex, type of surgery of the patient, co-morbidity if any size of ETT, the time of commencement of humidification , duration of use of humidifier, time of extubation, any complication leading to discontinuation of humidifier, frequency of refilling of nebulizer chamber, volume of ETT before intubation etc. will be noted.

The amount of Endotracheal tube blockade caused by secretion will be measured immediately following extubation.

The volume of Endotracheal tube secretion / amount of blockade will be assessed by the following process-

• The bevel end & Murphy's eye of the Endotracheal tube will be sealed using sterile insulating tape so that it become water tight. The tube will be gradually filled with measured amount of sterile fluid using small volume syringe to increase the accuracy of measurement. The amount of fluid it can hold will be measured & noted.

• The volume of extubated tube will be measured in the similar way.

• The measured volume of the Extubated Endotracheal tube will be subtracted from the actual volume of the particular Sized ETT ( measured before intubation).

• The result obtained after this subtraction will be the volume of secretion or the volume of ETT that has been blocked.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: January 2017
• Est. primary completion date: November 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. American Society of Anaesthesiologists (ASA) 1 and 2 adult Patients

2. Undergoing surgery for head and neck cancer

3. Requiring overnight endotracheal tube & breathing spontaneously

Exclusion Criteria:

1. Patients with major cardiac diseases( coronary artery disease, Valvular diseases)

2. Patients having gross chronic Obstructive Pulmonary Disease (COPD), bronchiectasis, cystic fibrosis.

3. Smokers(abstinence period less than 3 months)

4. Patient in drugs having sialogogue properties.

5. Patient on drugs having anti-sialogogue properties

Related Conditions & MeSH terms

• Cancer of Head and Neck
• Head and Neck Neoplasms

Intervention

Device:
• heated humidifier
30 patients requiring overnight intubation but breathing spontaneously without ventilatory support will be supplied humidified oxygen using Heated Humidifier(HH)
• mist humidifier
30 patients requiring overnight intubation but breathing spontaneously without ventilatory support will be supplied humidified oxygen using mist humidifier

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Tata Memorial Hospital

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Extent of Blockade of Endotracheal Tube Assessed by Change in the Endotracheal Tube Volume	The bevel end & Murphy's eye of the Endotracheal tube was sealed using sterile insulating tape so that it becomes water tight. The tube was gradually filled with measured amount of sterile fluid using small volume syringe to increase the accuracy of measurement. The amount of fluid it can hold was measured & noted	At baseline just before intubation and 24 hours from time of ICU admission
Primary	Assess the Increase in Nurses Work Load	Investigators will assess nursing workload by frequency of filling of humidifier chamber.	At baseline just before intubation and 24 hours from time of ICU admission