Intravenous Lidocaine and Alfentanil for Cough Prevention in Bronchoscopic Procedures
The study aims to evaluate the effectiveness of intravenous lidocaine and alfentanil in preventing cough during bronchoscopic procedures by analyzing cough severity, analgesia-nociception monitor scores, and EEG monitor levels.
bronchoscopic insertion
Cough+6
+ Lung Diseases
+ Pathologic Processes
Prevention Study
Summary
Study start date: May 9, 2022
Actual date on which the first participant was enrolled.The study investigates the effects of adding two drugs, lidocaine and alfentanil, given intravenously before a bronchoscopy procedure. This procedure often causes patients to cough, which can lead to complications like airway spasms or interruptions during the procedure. The research focuses on people undergoing bronchoscopic interventions without endotracheal tubes, where steady airways are crucial. The goal is to see if these medications can effectively reduce cough and improve the procedure's success, addressing a common problem faced during bronchoscopic procedures. Participants in the study receive either lidocaine, alfentanil, or a saline solution injected into their veins one minute before the bronchoscope is inserted. Researchers then record various responses including the severity of cough, visibility during the procedure, and reactions of the vocal cords. They also measure levels of anesthesia, pain response, blood pressure, heart rate, and oxygen levels in the blood. By evaluating these factors, the study aims to determine if these drugs can reduce cough intensity and improve patient stability during the procedure.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.108 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Prevention Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 20 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: * patients planned to receive bronchoscopic interventions for lung tumors with intravenous anesthesia. Exclusion Criteria: * conventional bronchoscopy without interventions such as EBUS, tracheal tumore excision
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.3 intervention groups are designated in this study
33.333% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorGroup III
PlaceboStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
National Taiwan University Cancer Center Hospital
Taipei, TaiwanOpen National Taiwan University Cancer Center Hospital in Google Maps