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Validity of Sputum Induction Method for the Diagnosis of Lung Cancer

Validity of Sputum Induction Method for the Diagnosis of Lung Cancer - Sputum Induction in Patients with Lung Cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004914
Enrollment
100
Registered
2011-01-21
Start date
2010-12-01
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

Patients with suspected lung cancer

Interventions

Spontaneous sputum cytology specimens were collected from each subject for 3 days after registration. On each day during the subsequent 3-day period, each subject was asked to inhale nebulized 10% hyp

Sponsors

National Hospital Organization Asahikawa Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with suspected lung cancer based on the detection of an abnormal opacity on the chest X-ray. Written informed consent

Exclusion criteria

Exclusion criteria: (1) patients with uncontrolled asthma, (2) patients with severe hepatopathy, nephropathy, cardiac disease or hematological disease, or other serious complications, (3) pregnant or possibly pregnant women, and (4) other patients judged by the physician as being unsuitable candidates for the study.

Design outcomes

Primary

MeasureTime frame
Sputum expectoration rate

Secondary

MeasureTime frame
1. Cytological examination of sputum induced by 10% hypertonic saline 2. Analysis of adverse events arising from the inhalation of 10% hypertonic saline 3. Testing of the lung carcinoma cells for EGFR gene mutation in sputum cytology-positive cases and comparison of the test results between spontaneous and induced sputum specimens 4. Questionnaire survey of the patients.

Countries

Japan

Contacts

Public ContactYuka Fujita

National Hospital Organization Asahikawa Medical Center Respiratory Medicine

yuka@asahikawamc.hosp.go.jp0166-51-3161

Outcome results

None listed

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