search
Back to results

Comparison of Three Different Puncture Techniques in EBUS-TBNA

Primary Purpose

Lung Cancer, Sarcoidosis, Tuberculosis

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Endobronchial ultrasound-guided transbronchial needle Slow-pull capillary sampling
Endobronchial ultrasound-guided transbronchial needle aspiration
Endobronchial ultrasound-guided transbronchial needle capillary sampling
Sponsored by
Beijing Friendship Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Lung Cancer

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age 18-80years Chest computed tomography showing hilar or mediastinal lymph node enlargement No contraindications for bronchoscopy Signed informed consent provided by the patient Disease needs to be diagnosed through the EBUS-TBNA Exclusion Criteria: Severe coagulation dysfunction Severe cardiopulmonary dysfunction Acute asthma attack or massive haemoptysis Poor general condition Physical weakness without tolerance for anaesthesia or allergy to narcotic drug Disease can be diagnosed by other less invasive methods (such as skin or peripheral superficial lymph node biopsy)

Sites / Locations

  • Beijing Friendship Hospital, Capital Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

EBUS-TBNSP

EBUS-TBNA

EBUS-TBNCS

Arm Description

The slow-pull capillary technique was performed as follows: after identification and measurement of the target lymph node, a needle was used to puncture the lymph node with the stylet in place.At the same time, the stylet was slowly and continuously pulled to create weak negative pressure.

The operation steps are the same as above, but the negative pressure device of 10ml syringe is connected behind the puncture needle.

The operation steps are the same as above, but there is no negative pressure device behind the puncture needle

Outcomes

Primary Outcome Measures

Diagnostic accuracy of three different puncture methods according to pathological diagnosis
The final pathological diagnosis was based on all available cytological and histological samples. In cases with negative pathological results , we continue to follow up the patients for ⩾6months.

Secondary Outcome Measures

Blood contamination of samples
Blood contamination was categorized as follows: low (no or few blood cells influencing the diagnosis), moderate (sample partially obscured by blood cells, but pathological diagnosis possible), and high (large numbers of blood cells, rendering pathological diagnosis difficult)
Bleeding of operation
There are three levels of bleeding:Small amount of bleeding(Ⅰ): Bleeding can stop spontaneously without continuous suction.Moderate bleeding(Ⅱ): Continuous suction is required, and epinephrine or ice salt water is used locally to stop bleeding.Massive bleeding(Ⅲ): Patients who need to be used balloon compression, interventional treatment, or blood transfusion treatment or even died of asphyxia due to bleeding.
Acquisition of tissue core of three different puncture methods according to the judgment of the pathologist
Tissue cores were immersed in formalin solution and subjected to histopathological examination. In the absence of a tissue core, the contents were pressed onto a glass slide, immersed in 96% methanol for ⩾10min and subjected to cytopathological examination.Some methods may only obtain cytological specimens, while others may obtain tissue cores. Tissue cores are better for pathologists to diagnose.

Full Information

First Posted
November 6, 2022
Last Updated
November 24, 2022
Sponsor
Beijing Friendship Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT05628454
Brief Title
Comparison of Three Different Puncture Techniques in EBUS-TBNA
Official Title
Comparison of Three Different Puncture Techniques in EBUS-TBNA
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 1, 2022 (Actual)
Primary Completion Date
November 1, 2024 (Anticipated)
Study Completion Date
November 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Beijing Friendship Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The purpose of this study was to compare the accuracy and sensitivity of slow-pull capillary technique, traditional suction aspiration and non negative pressure puncture in the diagnosis of mediastinal and/or hilar lymph node enlargement by ultrasound bronchoscopic lymph node biopsy.
Detailed Description
EBUS-TBNA has been widely used in the diagnosis of diseases involving lung hilar and mediastinal lymph node enlargement.But different puncture methods are still controversial. Research shows that there was no significant difference in sample adequacy, diagnostic specificity and accuracy between the no negative pressure aspiration and traditional negative pressure aspiration technique.Slow-pull capillary technique is a relatively new operating method of endoscopic ultrasound guided fine needle biopsy in recent years. At present, this technology is widely used in pancreatic space occupying lesions. Compared with the traditional negative pressure aspiration method, our previous retrospective study found that the slow-pull capillary technique can improve the diagnostic accuracy of patients. Therefore, the purpose of this study is to prospectively and randomly compare the advantages and disadvantages of three puncture methods in EBUS-TBNA.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer, Sarcoidosis, Tuberculosis

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Masking Description
The operator knows which puncture technique to be used, but the subject and the outcomes assessor does not know the technique.
Allocation
Randomized
Enrollment
75 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
EBUS-TBNSP
Arm Type
Experimental
Arm Description
The slow-pull capillary technique was performed as follows: after identification and measurement of the target lymph node, a needle was used to puncture the lymph node with the stylet in place.At the same time, the stylet was slowly and continuously pulled to create weak negative pressure.
Arm Title
EBUS-TBNA
Arm Type
Experimental
Arm Description
The operation steps are the same as above, but the negative pressure device of 10ml syringe is connected behind the puncture needle.
Arm Title
EBUS-TBNCS
Arm Type
Experimental
Arm Description
The operation steps are the same as above, but there is no negative pressure device behind the puncture needle
Intervention Type
Procedure
Intervention Name(s)
Endobronchial ultrasound-guided transbronchial needle Slow-pull capillary sampling
Other Intervention Name(s)
Slow-pull capillary technique
Intervention Description
The slow-pull capillary technique was performed as follows: after identification and measurement of the target lymph node, a needle was used to puncture the lymph node with the stylet in place.At the same time, the stylet was slowly and continuously pulled to create weak negative pressure.
Intervention Type
Procedure
Intervention Name(s)
Endobronchial ultrasound-guided transbronchial needle aspiration
Other Intervention Name(s)
Standard suction
Intervention Description
The operation steps are the same as above, but the negative pressure device of 10ml syringe is connected behind the puncture needle.
Intervention Type
Procedure
Intervention Name(s)
Endobronchial ultrasound-guided transbronchial needle capillary sampling
Other Intervention Name(s)
Fine needle sampling without suction
Intervention Description
The operation steps are the same as above, but there is no negative pressure device behind the puncture needle
Primary Outcome Measure Information:
Title
Diagnostic accuracy of three different puncture methods according to pathological diagnosis
Description
The final pathological diagnosis was based on all available cytological and histological samples. In cases with negative pathological results , we continue to follow up the patients for ⩾6months.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Blood contamination of samples
Description
Blood contamination was categorized as follows: low (no or few blood cells influencing the diagnosis), moderate (sample partially obscured by blood cells, but pathological diagnosis possible), and high (large numbers of blood cells, rendering pathological diagnosis difficult)
Time Frame
1 week
Title
Bleeding of operation
Description
There are three levels of bleeding:Small amount of bleeding(Ⅰ): Bleeding can stop spontaneously without continuous suction.Moderate bleeding(Ⅱ): Continuous suction is required, and epinephrine or ice salt water is used locally to stop bleeding.Massive bleeding(Ⅲ): Patients who need to be used balloon compression, interventional treatment, or blood transfusion treatment or even died of asphyxia due to bleeding.
Time Frame
1 week
Title
Acquisition of tissue core of three different puncture methods according to the judgment of the pathologist
Description
Tissue cores were immersed in formalin solution and subjected to histopathological examination. In the absence of a tissue core, the contents were pressed onto a glass slide, immersed in 96% methanol for ⩾10min and subjected to cytopathological examination.Some methods may only obtain cytological specimens, while others may obtain tissue cores. Tissue cores are better for pathologists to diagnose.
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-80years Chest computed tomography showing hilar or mediastinal lymph node enlargement No contraindications for bronchoscopy Signed informed consent provided by the patient Disease needs to be diagnosed through the EBUS-TBNA Exclusion Criteria: Severe coagulation dysfunction Severe cardiopulmonary dysfunction Acute asthma attack or massive haemoptysis Poor general condition Physical weakness without tolerance for anaesthesia or allergy to narcotic drug Disease can be diagnosed by other less invasive methods (such as skin or peripheral superficial lymph node biopsy)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xin He
Phone
0086-15801309510
Email
cynthia_cruise@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yanjun Wu
Organizational Affiliation
Beijing Friendship Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Zhigang Yao
Organizational Affiliation
Beijing Friendship Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Beijing Friendship Hospital, Capital Medical University
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100050
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ganggang Yu
Phone
0086-13717970816
Email
gangyu.603@163.com

12. IPD Sharing Statement

Learn more about this trial

Comparison of Three Different Puncture Techniques in EBUS-TBNA

We'll reach out to this number within 24 hrs