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Sedation Strategies for Diagnostic Bronchoscopy

The Effect and Safety of Different Sedation Strategies for Diagnostic Bronchoscopy

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03406533
Enrollment
28
Registered
2018-01-23
Start date
2018-02-01
Completion date
2018-03-31
Last updated
2019-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchoscopy, Sedation

Brief summary

Diagnostic bronchoscopy is an invasive procedure performed to diagnose respiratory diseases. But pain has been complained by most of the patients receiving such procedures. Sedation or anesthesia was required by both of the patients and bronchoscopists. Unfortunately, no consensus has been made upon the sedation strategies. Multiple sedation approaches have been applied, such as midazolam and fentanyl, remifentanil and propofol, dexmedetomidine and propofol. The present study was designed to compare these protocols in sedation for diagnostic bronchoscopy.

Interventions

DRUGMidazolam

Midazolam is used as a common medication for sedation in all groups.

DRUGDexmedetomidine

Dexmedetomidine is used for sedation in bronchoscopy with less impact on respiration.

DRUGRemifentanil

Remifentanil is used for analgesia to prevent bronchoscopy induced cough.

DRUGFentanyl

Fentanyl is another opioid drug used for analgesia to prevent bronchoscopy induced cough.

DRUGPropofol

Propofol is used for sedation with high efficacy but more side effect on respiration than dexmedetomidine.

Sponsors

Shanghai Zhongshan Hospital
CollaboratorOTHER
Ruijin Hospital
CollaboratorOTHER
Shanghai Pulmonary Hospital, Shanghai, China
CollaboratorOTHER
Changhai Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Scheduled for flexible diagnostic bronchoscopy * Adult patients aged 18 to 65 years * American Society of Anesthesiologists (ASA) Physical Status Classification I-II * BMI 18.5-25kg/m2 * Subjects provide informed consent

Exclusion criteria

* Severe airway obstruction * Coagulation disorder * Repeat bronchoscopy (more than 3 times) * Severe liver and renal dysfunction * Cardiovascular and cerebrovascular diseases * Pregnancy * Chronic opioid user * Drug abusers or addicts

Design outcomes

Primary

MeasureTime frameDescription
Cough scoreFrom the completion of local anesthesia with lidocaine to the completion of bronchoscopy procedure, assessed up to 2 hoursCough score across the procedure will be classified into 4 degree (1-4) as follows. 1 = none, 2 = one gag or cough only, 3 = \>1 gag or cough, but acceptable conditions, 4 = unacceptable conditions

Secondary

MeasureTime frameDescription
Body movementFrom the completion of local anesthesia with lidocaine to the completion of bronchoscopy procedure, assessed up to 2 hoursThe numbers of the times of any body movement across the procedure
Satisfaction score of the patients and bronchoscopistsAcross the procedure, assessed up to 2 hoursSatisfaction score of the patients and bronchoscopists regarding to the sedation quality measured by a 0-100 visual analogue scale (VAS). 100 refers to the highest satisfaction degree while 0 refers to the worst satisfaction degree.
Amount of the rescue use of propofolAfter sedation induction, assessed up to 2 hoursThe total amount of propofol used as a rescue therapy when the sedation is not deep enough as assessed by the anesthesiologists.
Recovery timeAfter termination of the sedation medication, assessed up to 2 hoursDuration of the recovery from sedation
Prevalence of the side effects of respiratory and circulatory systemAcross the sedation duration, assessed up to 2 hoursThe number of the side effects in respiratory and circulatory system during the procedure, including hypertension, hypotension, tackycardia, bradycardia, hypoxia and larynx spasm.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026