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Comparison of Procedural Yield of Bronchoalveolar Lavage Using Three Different Techniques in Subjects Undergoing Flexible Bronchoscopy (BAL-3T)

Primary Purpose

Bronchoalveolar Lavaage, Diffuse Lung Disease

Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Bronchoalveolar lavage using wall mount suction
Bronchoalveolar lavage using manual suction
Bronchoalveolar lavage using manual suction with rubber tubing
Sponsored by
Postgraduate Institute of Medical Education and Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Bronchoalveolar Lavaage

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients undergoing BAL procedure for various indications using flexible bronchoscopy

Exclusion Criteria:

  • Hemodynamic instability (SBP <90mmHg , Baseline Sp02 <92% on room air)
  • Failure to provide informed consent
  • Platelet count <20,000 per mm3
  • Pregnancy
  • Subjects already enrolled in any other study

Sites / Locations

  • Bronchoscopy suite, PGIMER
  • Bronchoscopy suite

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Manual suction

Manual suction with tubing

Wall mount suction

Arm Description

A 50-mL syringe will be used to apply the suction.

A 50-mL syringe with a 15-cm rubber tubing.

A negative pressure of <100 mmHg will be applied using continuous wall suction.

Outcomes

Primary Outcome Measures

To compare proportional procedures in which we obtain optimal yield
optimal yield will be defined if there is at least 30% return of volume instilled and adequate sample (<5% bronchial cells)

Secondary Outcome Measures

Diagnostic yield of BAL
Proportion of BAL in each arm that provide a specific diagnosis
Percentage and volume of BAL fluid
Percentage of instilled volume of saline for performing BAL that returns while doing BAL and the exact volume of BAL
Proportion of subjects experiencing complications in each arm
Complications will include hypoxemia, fever, escalation of care (need for hospitalization, icu admission or airway intubation), airway bleeding, death, and others

Full Information

First Posted
June 10, 2022
Last Updated
August 12, 2023
Sponsor
Postgraduate Institute of Medical Education and Research
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1. Study Identification

Unique Protocol Identification Number
NCT05425875
Brief Title
Comparison of Procedural Yield of Bronchoalveolar Lavage Using Three Different Techniques in Subjects Undergoing Flexible Bronchoscopy
Acronym
BAL-3T
Official Title
A Randomized Controlled Trial to Compare Procedural Yield of Bronchoalveolar Lavage Using Three Different Techniques in Subjects Undergoing Flexible Bronchoscopy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
June 1, 2022 (Actual)
Primary Completion Date
June 30, 2023 (Actual)
Study Completion Date
June 30, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Postgraduate Institute of Medical Education and Research

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Bronchoalveolar lavage (BAL) via flexible bronchoscopy is a method used to sample the cellular and microbiological components of the alveolar space. It is a procedure in which 2-3 measured aliquots of sterile normal saline are instilled after wedging the scope to the suitable segmental bronchus. BAL is performed from the segments/ lobes showing ground-glass opacities (GGO), tree-in-bud lesions or focal consolidations guided by HRCT. In diffuse lung involvement, BAL is performed either from RML or the lingula.[3] It is recovered through the bronchoscope via different suction methods so as to get a sample of epithelial lining fluid of small airways and alveoli. Either manual suction or wall suction can be used for aspiration of fluid during BAL. The fluid recovered is then sent for cytology and microbiology examination studies including AFB, MGIT, GeneXpert, Galactomannan, fungal cultures to diagnose various conditions like PAP, eosinophilic pneumonia, bacterial or fungal infections, specific forms of ILD. Three techniques have been described to perform BAL. To the best of our knowledge no previous study has compared the three methods of obtaining the BAL in the same cohort of subjects.The authors believe that the procedural yield of BAL will be best by manual suction using rubber tubing compared to manual suction without rubber tubing or wall suction. Herein, the investigators compare the three methods of obtaining BAL in subjects undergoing BAL for various respiratory diseases
Detailed Description
Bronchoalveolar lavage (BAL) via flexible bronchoscopy is a method used to sample the cellular and microbiological components of the alveolar space. It is a procedure in which 2-3 measured aliquots of sterile normal saline are instilled after wedging the scope to the suitable segmental bronchus. BAL is performed from the segments/ lobes showing ground-glass opacities (GGO), tree-in-bud lesions or focal consolidations guided by HRCT. In diffuse lung involvement, BAL is performed either from RML or the lingula.[3] It is recovered through the bronchoscope via different suction methods so as to get a sample of epithelial lining fluid of small airways and alveoli. Either manual suction or wall suction can be used for aspiration of fluid during BAL. The fluid recovered is then sent for cytology and microbiology examination studies including AFB, MGIT, GeneXpert, Galactomannan, fungal cultures to diagnose various conditions like PAP, eosinophilic pneumonia, bacterial or fungal infections, specific forms of ILD Normal BAL cellular components are specified as: Alveolar macrophages (AM) 85%, Lymphocytes 5-15%, Neutrophils <= 3%, eosinophils <1%. The presence of squamous epithelial cells indicates contamination by oropharyngeal secretions. [4] Additionally, BAL can be a tool for pulmonary toilet in rare diseases such as pulmonary alveolar proteinosis by helping to remove the abnormal surfactant material that accumulates with this disease. Manual suction: It can be done using the same syringe used for instillation of the normal saline. At least 100 ml normal saline should be instilled while performing BAL and should not exceed 200 ml. According to the studies, Modification of the manual suctioning technique (by connecting small tubing attached to syringe) provides higher percentage of BAL fluid [5]. Wall suction: During suctioning the instilled fluid, negative pressure is applied using continuous wall suction. The pressure should be <100mmHg or should be adjusted to prevent airway collapse.[6] In a study conducted by Aruna D. Herath[7], 73 pediatric patients were enrolled for a RCT undergoing flexible bronchoscopy and BAL. Two different suctioning techniques were compared for % of BAL fluid recovery. Sterile normal saline according to 1ml/kg was instilled and 100-150mmHg of negative pressure was applied for wall suction method. Thus it concluded that wall suction had better BAL fluid recovery than handheld syringe suction. Diagnostic yield was the same for both techniques. Luis M. Seijo[8], conducted a prospective randomized study of total 220 patients undergoing BAL. Study comparing manual and wall suction in performance of BAL resulted that manual aspiration is superior to wall suction yielding larger quantity of BAL. Additionally, extra tubing with 50 ml syringe was added in manual suction technique and 50mmHg negative pressure was used in wall suction method. A prospective clinical study of 66 patients by Naghmeh Radhakrishna[9], comparing techniques for optimal BAL performance used 100ml NS (with 4 aliquots) resulted in no significant difference between both techniques. Another study to compare two aspiration techniques of BAL in children was conducted by Christian Rosas-Salazar[10] on approximately 540 procedures. Their results suggested that handheld syringe suction provide higher % of fluid return when compared to continuous wall suction. K.S Woods[11], did a randomized, blinded prospective clinical trial on 18 dogs comparing manual and suction pump aspiration techniques for BAL. 35 ml syringe was used to instill 2ml/kg volumes per site for manual aspiration. Negative pressure of maximum 50mmHg was applied for SPA. Thus, concluded the study showing higher % of BALF return by SPA than manual suction with or without tubing. There was no significant difference in diagnostic yield. One more multicenter randomized study by Antoni Rosell[12] was conducted to recover BAL fluid comparing only syringe and syringe with attached plastic tube (40cm), for more fluid return. Thus, it resulted in 8% more fluid recovery, more yield and less complications with syringe with tubing suction technique. To the best of author's knowledge no previous study has compared the three methods of obtaining the BAL in the same cohort of subjects. The investigators believe that the procedural yield of BAL will be best by manual suction using rubber tubing compared to manual suction without rubber tubing or wall suction. Herein, the investigators compare the three methods of obtaining BAL in subjects undergoing BAL for various respiratory diseases. Study question: Is the procedural yield of BAL different between manual suction using rubber tubing compared to manual suction without rubber tubing or wall suction?

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bronchoalveolar Lavaage, Diffuse Lung Disease

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Three arm parallel group study
Masking
Investigator
Masking Description
Investigator will be blinded to the group allotment
Allocation
Randomized
Enrollment
942 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Manual suction
Arm Type
Experimental
Arm Description
A 50-mL syringe will be used to apply the suction.
Arm Title
Manual suction with tubing
Arm Type
Experimental
Arm Description
A 50-mL syringe with a 15-cm rubber tubing.
Arm Title
Wall mount suction
Arm Type
Active Comparator
Arm Description
A negative pressure of <100 mmHg will be applied using continuous wall suction.
Intervention Type
Procedure
Intervention Name(s)
Bronchoalveolar lavage using wall mount suction
Intervention Description
BAL will be performed using wall mount suction with a pressure <100 mmHg
Intervention Type
Procedure
Intervention Name(s)
Bronchoalveolar lavage using manual suction
Intervention Description
A 50-mL syringe will be used to apply suction through the working channel of a bronchoscope
Intervention Type
Procedure
Intervention Name(s)
Bronchoalveolar lavage using manual suction with rubber tubing
Intervention Description
A 50-mL syringe with an attached rubber tubing will be used to apply suction through the working channel of a bronchoscope
Primary Outcome Measure Information:
Title
To compare proportional procedures in which we obtain optimal yield
Description
optimal yield will be defined if there is at least 30% return of volume instilled and adequate sample (<5% bronchial cells)
Time Frame
1 hour (during bronchsocopy)
Secondary Outcome Measure Information:
Title
Diagnostic yield of BAL
Description
Proportion of BAL in each arm that provide a specific diagnosis
Time Frame
1 month
Title
Percentage and volume of BAL fluid
Description
Percentage of instilled volume of saline for performing BAL that returns while doing BAL and the exact volume of BAL
Time Frame
1 hour (during bronchsocopy)
Title
Proportion of subjects experiencing complications in each arm
Description
Complications will include hypoxemia, fever, escalation of care (need for hospitalization, icu admission or airway intubation), airway bleeding, death, and others
Time Frame
1 month after the procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients undergoing BAL procedure for various indications using flexible bronchoscopy Exclusion Criteria: Hemodynamic instability (SBP <90mmHg , Baseline Sp02 <92% on room air) Failure to provide informed consent Platelet count <20,000 per mm3 Pregnancy Subjects already enrolled in any other study
Facility Information:
Facility Name
Bronchoscopy suite, PGIMER
City
Chandigarh
ZIP/Postal Code
160012
Country
India
Facility Name
Bronchoscopy suite
City
Chandigarh
ZIP/Postal Code
160012
Country
India

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Data sharing

Learn more about this trial

Comparison of Procedural Yield of Bronchoalveolar Lavage Using Three Different Techniques in Subjects Undergoing Flexible Bronchoscopy

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