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To assess the usefulness of new EBUS-TBNA needle.

To assess the usefulness of new EBUS-TBNA needle. - To assess the usefulness of new EBUS-TBNA needle.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000031291
Enrollment
40
Registered
2018-02-20
Start date
2018-02-20
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-small cell lung cancer with advanced stage

Interventions

None listed

Sponsors

National Cancer Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with enlarged mediastinal and/or hilar lesions 10 mm or greater in short-axis diameter on CT or FDG uptaken 2.5 or higher in PET/CT imaging requiring diagnostic EBUS-TBNA 2. 20 years old and above 3. Informed consent

Exclusion criteria

Exclusion criteria: 1.Patients requiring EBUS-TBNA for N-stage in patients with lung cancer 2.Serious concomitant medical illness

Design outcomes

Primary

MeasureTime frame
Yields of adequate tissue specimen sampling

Countries

Japan

Contacts

Public ContactToshiyuki Nakai

National Cancer Center Hospital Department of Endoscopy, Respiratory Endoscopy Division

tnakai@ncc.go.jp03-3542-2511

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026