Raman Spectroscopic Analysis of Bronchoscopic Biopsy for Diagnosing Lung Cancer

NCT ID: NCT05799027

Last Updated: 2023-04-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-03-31

Study Completion Date

2024-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Lung Cancer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Raman spectrum analysis

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

Group Type EXPERIMENTAL

Raman spectrum

Intervention Type DIAGNOSTIC_TEST

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

Interventions

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Raman spectrum

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

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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China-Japan Friendship Hospital

OTHER

Sponsor Role lead

Responsible Party

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Gang Hou

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Mingming Deng, MD

Role: CONTACT

86 18801336854

Other Identifiers

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2022-NHLHCRF-LX-01-0201-05

Identifier Type: -

Identifier Source: org_study_id

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