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Efficacy of Pre-intubation Chlorhexidine Oral Care on Health Outcomes

Surgery Clinical Trial

Official title:
Efficacy of Pre-intubation Chlorhexidine Oral Care on Health Outcomes

Clinical Trial Summary

This single-centre, single-blind, randomised controlled study with parallel-group design was conducted in Yun Ling, Taiwan between May 2019 and August 2019. Participants were randomly allocated to an intervention (mouth care using 0.12% CHX before intubation) or control (standard care) group on a 1:1 basis. This study was approved by the institutional review board of National Taiwan University Hospital, Taiwan (IRB No.201806086RINB). Each participant completed written informed consent after explanation of this study and advised that they could withdraw anytime.

Clinical Trial Description

Participants were recruited at the operation room of a teaching hospital. Participants were included if they met the following criteria: 18-80 years of age, American Society of Anesthesiologists, ASA) class 1-3, scheduled for surgery under endotracheal tube intubation general anesthesia. Patients were excluded if they were diagnosed with upper or lower respiratory tract disease, including COPD, cold, had oral ulcer, scheduled to have a respiratory-related surgical procedure, had endotracheal tube intubated. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04252469
Study type Interventional
Source National Taiwan University Hospital
Contact
Status Completed
Phase N/A
Start date May 1, 2019
Completion date August 31, 2019
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