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NCT03903471

22G-ProCore vs 22G-Standard Needle in Diagnosis of Lymphadenopathy by EBUS-TBNA

Status unknown NA Last updated 29 September 2022
What this trial tests

NA trial testing 22G-ProCore Endobronchial Ultrasound Needle in Lymph Node Disease in 600 participants. Status unknown.

Timeline
8 October 2022
Primary endpoint
8 October 2023
8 October 2023

Quick facts

Lead sponsorJiayuan Sun
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposediagnostic
Enrollment600
Start date8 October 2022
Primary completion8 October 2023
Estimated completion8 October 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Jiayuan Sun

Who can join

18 and older, any sex, with Lymph Node Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study is to compare the performance of 22G-ProCore and 22G-Standard needle in diagnosis of mediastinal and hilar lymphadenopathy via EBUS-TBNA with the purpose to explore the optimal technique for obtaining diagnostic material.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Jiayuan Sun trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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