Completed

Intravenous Lidocaine and Alfentanil for Cough Prevention in Bronchoscopic Procedures

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Study Aim

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.

What is being tested

bronchoscopic insertion

Procedure
Who is being recruted

Cough+6

+ Lung Diseases

+ Pathologic Processes

From 20 to 65 Years
See all eligibility criteria
How is the trial designed

Prevention Study

Placebo-Controlled
Interventional
Study Start: May 2022
See protocol details

Summary

Principal SponsorNational Taiwan University Hospital
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleEffects of Adding Intravenous Lidocaine, Alfentanil Before Bronchoscopic Insertion for Preventing Cough During Bronchoscopic Spraying of Local Anesthetics in Non-intubated Bronchoscoopic Interventions
NCT05072236
Principal SponsorNational Taiwan University Hospital
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

108 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

CoughLung DiseasesPathologic ProcessesRespiration DisordersRespiratory Tract DiseasesSigns and SymptomsSigns and Symptoms, RespiratoryPathological Conditions, Signs and SymptomsRespiratory Aspiration

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.
Treatment Groups
Study Objectives

3 intervention groups are designated in this study

33.333% chance of being blinded to the placebo group

Treatment Groups

Group I

Experimental
intravenous alfentanil 10 ug/kg 1 minute before bronchoscope insertion

Group II

Active Comparator
intravenous lidocaine 1.5 mg/kg 1 minute before bronchoscope insertion

Group III

Placebo
intravenous normal saline 5 mL 1 minute before bronchoscope insertion

Study 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

Suspended

National Taiwan University Cancer Center Hospital

Taipei, TaiwanOpen National Taiwan University Cancer Center Hospital in Google Maps
CompletedOne Study Center