Utility of Syringe Based Suction Versus Channel Suction in Bronchoalveolar Lavage
NCT ID: NCT01853904
Last Updated: 2014-01-07
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.
COMPLETED
NA
50 participants
INTERVENTIONAL
2012-07-31
2013-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The investigators concern is that channel suction creates too much force and there is collapsing of the airways which results in decreased fluid removal as well as cell sampling. The investigators propose that syringe based suctioning will not only return more of the instilled fluid but also more cells from the alveoli.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
May Noninvasive Mechanical Ventilation (NIV) and/or Continuous Positive Airway Pressure (CPAP) Increase the Bronchoalveolar Lavage (BAL) Salvage in Patients With Pulmonary Diseases?
NCT05631132
Comparison of Two Strategies of Oropharyngeal and Tracheal Suctioning in Mechanically Ventilated Patients
NCT01807884
Oral Suction Intervention to Reduce Aspiration and Ventilator Events: NO-ASPIRATE
NCT02284178
Does Tracheal Suction During Extubation in Intensive Care Unit Decrease Functional Residual Capacity
NCT03681626
Aspiration in Acute Respiratory Failure Survivors
NCT02363686
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Channel Suction first
This arm is for patients who will receive channel suction first to obtain the specimen then syringe suction to obtain the specimen.
Bronchoscopy/ BAL with Channel Suction
The wall suction used for the channel suction will be set at 80 mm Hg. This arm is for patients who will receive channel suction first to obtain the specimen then syringe suction to obtain the specimen.
Bronchoscopy/BAL with Syringe Suction
Syringe based suctioning will be performed with 20mL syringe.
Syringe Suction first
This arm is for patients who will receive syringe suction first to obtain the specimen then channel suction to obtain the specimen.
Bronchoscopy/ BAL with Channel Suction
The wall suction used for the channel suction will be set at 80 mm Hg. This arm is for patients who will receive channel suction first to obtain the specimen then syringe suction to obtain the specimen.
Bronchoscopy/BAL with Syringe Suction
Syringe based suctioning will be performed with 20mL syringe.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Bronchoscopy/ BAL with Channel Suction
The wall suction used for the channel suction will be set at 80 mm Hg. This arm is for patients who will receive channel suction first to obtain the specimen then syringe suction to obtain the specimen.
Bronchoscopy/BAL with Syringe Suction
Syringe based suctioning will be performed with 20mL syringe.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Oklahoma
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Brent Brown, MD
Role: PRINCIPAL_INVESTIGATOR
OUHSC
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
OUHSC
Oklahoma City, Oklahoma, United States
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.
2296
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.