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The prospective randomized controlled trial of endbronchial ultrasound-guided transbronchial needle aspiration using 22G and 25G aspiration needles for lung cancer

Not Applicable
Recruiting
Conditions
ung cancer
Registration Number
JPRN-UMIN000036680
Lead Sponsor
ational Cancer Center Hospital East Depertment of Thoracic Oncology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

1.Patients who need multiple lymph node punctures. 2.Patients with hypersensitivity to lidocaine, midazolam, flumazenil, pethidine hydrochloride, or patients with severe hypersensitivity to other drugs. 3.Patients who have clinical symptoms that are interfere in performing bronchoscopy. 4.Patients using antiplatelet drugs or anticoagulants. (It is acceptable if there is an appropriate withdrawal period) 5.Patients judged to be inappropriate by the attending physician. 6.Patients who have participated in this study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The result of comparing of the the diagnostic accuracy of EBUS-TBNA with a 22-gauge and a 25-gauge aspiration needle in the historogically diagnosis of malignant tumor
Secondary Outcome Measures
NameTimeMethod
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