Ignite Creation Date:
2024-05-06 @ 8:07 PM
Last Modification Date:
2024-10-26 @ 3:21 PM
Study NCT ID:
NCT06262620
Status:
RECRUITING
Last Update Posted:
2024-02-16
First Post:
2024-02-01
Brief Title:
The Comparison of EBUS-TBNA TBMC Via a Tunnel and TBFB Via a Tunnel in Diagnosing Mediastinal Lymphadenopathy
Sponsor:
China-Japan Friendship Hospital
Organization:
China-Japan Friendship Hospital
Study Overview
Official Title:
The Comparison of Endobronchial Ultrasound-guided Transbronchial Needle Aspiration Mediastinal Cryobiopsy Via a Tunnel and Forceps Biopsy Via a Tunnel in Diagnosing Mediastinal Lymphadenopathy a Multicenter Randomised Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this prospective multi-centre randomised controlled clinical study is to compare the diagnostic yield and safety of the three biopsy techniques EBUS-TBNA EBUS-TBMC via a tunnel and EBUS-TBFB via a tunnel in mediastinalhilar lymph node biopsies
Participants will divided into EBUS-TBNA group EBUS-TBMC via a tunnel group and EBUS-TBFB via a tunnel group at a 111 ratio by using central computerized random sequence and then undertake EBUS-TBNA EBUS-TBMC via a tunnel or EBUS-TBFB according to the group
Researchers will compare the diagnostic yield and incidence of adverse events of the three biopsy techniques
Participants will divided into EBUS-TBNA group EBUS-TBMC via a tunnel group and EBUS-TBFB via a tunnel group at a 111 ratio by using central computerized random sequence and then undertake EBUS-TBNA EBUS-TBMC via a tunnel or EBUS-TBFB according to the group
Researchers will compare the diagnostic yield and incidence of adverse events of the three biopsy techniques
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None