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Diagnostic feasibility using a new cryoprobe for peripheral pulmonary lesions

An observational study: the diagnostic feasibility using a new single-use cryoprobe for peripheral pulmonary lesions

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1032200065
Enrollment
50
Registered
2020-07-08
Start date
2020-07-15
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

Lung neoplasms Lung neoplasms

Interventions

None listed

Sponsors

Tanaka Midori
Lead Sponsor
Matsumoto Yuji
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients planning to undergo cryobiopsy for peripheral pulmonary lesions suspected of lung malignant neoplasms based on clinical signs and radiological images 2) Patients with a high-resolution CT scan performed within 1 month of the entry and the images fulfill the following three points i) A long diameter of 30 mm or less on the axial view ii) A solitary pulmonary nodule iii) A lesion locating beyond the subsegmental bronchus 3) Patients with no treatment history (i.e., surgery, radiation therapy, antitumor drugs, and so on) for the target lesion 4) Patients not younger than 20-year-old at the time of informed consent 5) Patients discontinuing anticoagulants and/or antiplatelet agents if used 6) Patients providing written informed consent

Exclusion criteria

Exclusion criteria: 1) Patients with a treatment history (i.e., surgery, radiation therapy, antitumor drugs, and so on) for the same side as the target lesion 2) Patients with a tracheostoma 3) Patients with poorly controlled mental disorders and/or dementia 4) Patients deemed unsuitable for inclusion in the study for any other reason based on the assessment by the investigators

Design outcomes

Primary

MeasureTime frame
diagnostic yield (sensitivity)

Secondary

MeasureTime frame
safety, specificity and accuracy, procedure duration, diagnostic yield by each sampling, microscopic evaluation for each tissue sample, diagnostic possibility by each tissue sample, and cumulative sensitivity

Contacts

Public ContactMidori Tanaka

National Cancer Center Hospital

midotana@ncc.go.jp+81-3-3542-2511

Outcome results

None listed

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