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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05799027
Other study ID # 2022-NHLHCRF-LX-01-0201-05
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 31, 2023
Est. completion date December 31, 2024

Study information

Verified date March 2023
Source China-Japan Friendship Hospital
Contact Mingming Deng, MD
Phone 86 18801336854
Email isdeng1017@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to evaluate raman spectroscopic analysis of bronchoscopic biopsy for diagnosing lung cancer in visible lesions in the airway. The main question it aims to answer are: the diagnostic efficacy raman spectroscopic analysis of bronchoscopic biopsy for diagnosing lung cancer. The bronchoscopic biopsy sample of patients with visible lesions in the airway would undergo raman spectrum analysis.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Patients who plan to undergo bronchoscopic biopsy or EBUS-TBNA - Visible intratracheal lesions under bronchoscope - Non-visible lesions suspected of lung cancer Exclusion Criteria: - The patient could not tolerate further examination aimed at clarifying the cause of the disease or refused to accept further examination aimed at clarifying the cause of the disease due to poor general condition, serious organ dysfunction, etc - The patient has no definite diagnosis

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Raman spectrum
The bronchoscopic biopsy sample of patients with visible lesions in the airway would undergo raman spectrum analysis.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
China-Japan Friendship Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary To establish the sensitivities and specificities of Raman spectroscopic analysis of bronchoscopic biopsy for lung cancer. The diagnosis would be confirmed according to the pathological results. 7 days after the biopsy
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