Impact of Current Smoking in the Tolerance of Bronchoscopy
NCT ID: NCT01345383
Last Updated: 2015-03-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
TERMINATED
100 participants
OBSERVATIONAL
2010-06-30
2013-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Etiologies, Investigations and Outcomes of Patients Presenting With Hemoptysis
NCT02913365
Effects of Smoking on Bronchial Epithelium
NCT00849433
EFFECT OF SMOKING ON MUCUS HYPERSECRETION MECHANISMS IN ASTHMA AND CHRONIC OBSTRUCTIVE PULMONARY DISEASE
NCT01947218
Cryoprobe Transbronchial Lung Biospy in Patients With Mechanical Ventilation
NCT02611297
Epidemiology of Chronic Bronchitis in Patients With Chronic Obstructive Pulmonary Disease (COPD)
NCT02128529
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The investigators compare patients who did not smoke in the 6 hours before the bronchoscopy and those who have smoked.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Current smokers
bronchoscopy
Routine bronchoscopy under local anesthesia (lidocain). Duration: +/- 10 min
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
bronchoscopy
Routine bronchoscopy under local anesthesia (lidocain). Duration: +/- 10 min
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* bronchoscopy under local anesthesia
Exclusion Criteria
* intravenous sedative
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Centre Hospitalier Universitaire Saint Pierre
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Marie Bruyneel
Chef de clinique adjoint
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Isabelle De Meulder, MD
Role: PRINCIPAL_INVESTIGATOR
Centre Hospitalier Universitaire Saint Pierre
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
CHU Saint Pierre
Brussels, , Belgium
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AK/10-05-3898/38
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.