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Clinical Trials/NCT01345383
NCT01345383TerminatedNot Applicable

Impact of Current Smoking in the Tolerance of Bronchoscopy

Centre Hospitalier Universitaire Saint Pierre1 site in 1 country100 target enrollmentStarted: June 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
cough

Study Overview

Brief Summary

The purpose of this study is to study the impact of smoking in the preceding hours before a bronchoscopy on the tolerance of this exam.

Detailed Description

Tolerance evaluation of the bronchoscopy on current and regular smokers. The investigators assess episodes of cough, dyspnea, volume of lidocain (liquid 1% and in spray 10%), duration of the procedure, episodes of desaturation and completion of the bronchoscopy.

The investigators compare patients who did not smoke in the 6 hours before the bronchoscopy and those who have smoked.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • current and regular smoker
  • bronchoscopy under local anesthesia

Exclusion Criteria

  • patients needing EBUS or fluoroscopy
  • intravenous sedative

Outcomes

Primary Outcomes

cough

Time Frame: Day 1

number of cough episodes during the bronchoscopy

Secondary Outcomes

  • dyspnea(day 1)
  • Lidocaine volume(day 1)
  • length of bronchoscopy(Day 1)
  • desaturation episodes(day 1)

Investigators

Sponsor
Centre Hospitalier Universitaire Saint Pierre
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Marie Bruyneel

Chef de clinique adjoint

Centre Hospitalier Universitaire Saint Pierre

Study Sites (1)

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