The Affecting Factors on Airway Temperature and Moisture
The Effects of Different Fresh Gas Flows and Different Anesthetics on Airway Temperature and Moisture in Patients Who Underwent General Anesthesia
1 other identifier
observational
240
0 countries
N/A
Brief Summary
There is no literature information about the flow rate of fresh gas mixture (air+O2) in the patients who underwent general anesthesia. Different flow rates of fresh gas mixture are used in both the investigator's hospital and the experiences of the anesthesiologists. It is aimed to study the effects of different fresh gas flow rates on the rate of temperature and moisture of the airway of patients who underwent general anesthesia.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2016
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2018
CompletedFirst Submitted
Initial submission to the registry
December 17, 2019
CompletedFirst Posted
Study publicly available on registry
December 19, 2019
CompletedDecember 20, 2019
December 1, 2019
2 years
December 17, 2019
December 18, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Affect of two fresh gas flow rates (3lt/ 6lt min) on patients' airway temperature and humidity.
We will evaluate if different fresh gas flows effect on patients' airway temperature and moisture. We will evaluate by using a thermo-hygrometer fixed on anesthesia circuit.
2016-2018
Secondary Outcomes (1)
Affect of different anesthetic gases (sevoflurane, desflurane) and drugs (propofol)on patients' airway temperature and humidity.
2016-2018
Study Arms (2)
3 lt/min
Patients in the study were divided into two main groups according to the standard fresh gas flow administered (3-6 L/min). Each main group was then divided into subgroups as follows: sevoflurane + remifentanil, desflurane + remifentanil, or propofol + remifentanil (TIVA). These six groups were further divided into two groups according to use or non-use of a heat and moisture exchanger (HME) filter.
6 lt/min
Patients in the study were divided into two main groups according to the standard fresh gas flow administered (3-6 L/min). Each main group was then divided into subgroups as follows: sevoflurane + remifentanil, desflurane + remifentanil, or propofol + remifentanil (TIVA). These six groups were further divided into two groups according to use or non-use of a heat and moisture exchanger (HME) filter.
Interventions
Eligibility Criteria
Patients who were aged between 18-65 years and underwent surgery with general anesthesia.
You may qualify if:
- Patients aged 18-65 years underwent general anesthesia -
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (1)
Ozcan IG, Onal O, Ozdemirkan A, Saltali A, Sari M. Effects of different fresh gas flows and different anesthetics on airway temperature and humidity in surgical patients: a prospective observational study. Med Gas Res. 2022 Jul-Sep;12(3):83-90. doi: 10.4103/2045-9912.330691.
PMID: 34854418DERIVED
Study Officials
- PRINCIPAL INVESTIGATOR
Ozkan Onal, Professor
Selcuk University
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
December 17, 2019
First Posted
December 19, 2019
Study Start
April 1, 2016
Primary Completion
April 1, 2018
Study Completion
April 1, 2018
Last Updated
December 20, 2019
Record last verified: 2019-12
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
- Time Frame
- The IPD and any additional supporting information will become available in starting 2 months after publication.
The type(s) of supporting information that will be shared, in addition to the individual participant data set and data dictionaries for the IPD itself.