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Lung Cancer in Normal and Malignant TumorsSERS on lungNCT06775587

SERS-Based Serum Molecular Spectral Screening for Benign and Malignant Pulmonary Proliferative Nodules

An observational study of Lung Cancer in Normal and Malignant Tumors, run by Fuzhou General Hospital at 1 site in China.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Pulmonary nodules are often an early indicator of lung cancer. With the widespread adoption of chest CT scans in routine physical examinations, an increasing number of pulmonary nodules are being detected, including a variety of small nodules such as inflammatory lesions, benign tumors, and malignant tumors. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Serum Raman spectroscopy intelligent diagnostic system
How many people
200 participants
Where
1 siteChina
Study dates
8 Apr 2026to 31 Dec 2026
How long will I take part?
1 Year
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Chest CT reveals the presence of pulmonary nodules in the patient and plans to undergo surgical treatment

Who may be able to join

  • Participants with Lung cancer meeting the criteria of TNM (Ninth Edition);
  • Participants are willing to participate in this study and follow the research plan;
  • Participants or legally authorized representatives can give written informed consent approved by the Ethics Review Committee that manages the website.

Who cannot join

  • Participants with concomitant other malignant tumors;
  • Participants with missing baseline clinical data;
  • Participants with severe underlying lung diseases (such as bronchiectasis, bronchial asthma or COPD, etc.), or those with a history of occupational or environmental exposure to dust, mines or asbestos;
  • Participants who do not cooperate or refuse to participate in clinical trials at a later stage.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Zongyang Yu, Ph.D contact

13509327806

yuzy527@sina.com

China1 site
  • Raman detector

    Fuzhou, Fujian, 350000

    Zongyang Yu, degree, 0591-22859650, yuzy525@sina.com

Other trials in China

About this study

Official title: SERS-Based Serum Molecular Spectral Screening for Benign and Malignant Pulmonary Proliferative Nodules: A Multicenter, Open-Label, Double-Blind, Independent Data Analysis Clinical Trial

Pulmonary nodules are often an early indicator of lung cancer. With the widespread adoption of chest CT scans in routine physical examinations, an increasing number of pulmonary nodules are being detected, including a variety of small nodules such as inflammatory lesions, benign tumors, and malignant tumors. Currently, there is no unified international consensus on the diagnostic and treatment strategies for pulmonary nodules, as outlined by various global guidelines. Developing and implementing a comprehensive lung nodule and lung cancer screening program within public health management systems remains a complex and challenging endeavor. Advancing research and proposing lung cancer screening technologies that are highly sensitive, highly specific, simple, accessible, and cost-effective is an essential and pressing priority in modern healthcare.

Raman spectroscopy (RS), as a non-invasive and highly specific molecular detection technique, can be obtained at the molecular level to sensitively detect changes in biomolecules composed of proteins, nucleic acids, lipids, and sugars related to tumor metabolism in biological samples. The surface enhanced Raman spectroscopy (SERS) developed based on this technology is one of the feasible methods for high-sensitivity biomolecule analysis. Although SERS technology has shown good diagnostic efficacy in lots of preclinical studies in multiple tumors, it is limited to a generally small sample size and lacks external validation. There for, a clinical study of Raman spectra for tumor diagnosis is needed, which meets the following requirements: 1.An objective, fast and practical application of Raman spectral data processing is needed and deep learning method may be the best classification method; 2. It requires multicenter and large clinical samples to train deep learning diagnostic model, and verify its true efficacy through external data of prospective study.

In preliminary research, the investigators collected serum Raman spectroscopy data from a cohort of 191 patients with pulmonary nodules and developed an intelligent diagnosis system for distinguishing between benign and malignant pulmonary nodules using a machine learning model. The system achieved an accuracy of 89.7%. In order to obtain the highest level of clinical evidence and truly realize clinical transformation, this prospective, multi-center clinical study is designed to verify the intelligent diagnostic system for early diagnosis of prostate cancer.

Read the detailed description

In 2020, there were approximately 19.3 million new cancer cases and nearly 10 million cancer deaths worldwide. Among them, the number of new cases of lung cancer was approximately 2.21 million, accounting for 11.4% of the total number of new cancer cases. There were approximately 1.8 million deaths from lung cancer, ranking first among cancer deaths. In that year, the number of new cases of lung cancer in China was 816,000, accounting for 37% of the global total. In 2022, the latest number of lung cancer cases in China increased to 1.0606 million, and the number of lung cancer deaths was 733,000. In terms of the 5-year survival rate of lung cancer patients, the data released in 2018 in China (2012-2015) was 19.7%, which is still a large gap from the overall cancer 5-year survival rate of 46.6% by 2030 proposed in the "Healthy China Action-Cancer Prevention and Control Action Implementation Plan (2023-2030)". The prognosis of lung cancer at different stages is quite different. The 5-year survival rate of stage I lung cancer is 77%~92%, and the 5-year survival rate of stage IIIA~IVB lung cancer is 0~36%. Therefore, early diagnosis and treatment of lung cancer is the key to improving the 5-year survival rate of lung cancer and improving the prognosis of patients. However, most lung cancer patients are already in the late stage of lung cancer when they are diagnosed, and they have missed the opportunity for radical treatment. The main reason is that the primary and secondary prevention work is not done enough. It is necessary to develop advanced technologies and integrate them into the consensus guidelines for wide promotion.

Pulmonary nodules are early manifestations of lung cancer. With the popularization of chest CT screening in physical examination items, more and more lung nodules are found in physical examinations, including various types of small nodules, such as inflammatory lesions, benign tumor lesions, and malignant tumor lesions. In order to identify these types of nodules, clinicians often judge the two-dimensional imaging features of nodules based on their personal experience, such as plane diameter, whether there are burrs, lobes, calcification and other features to assess the probability of malignancy of lung nodules, but the accuracy of judging the benign and malignant nodules in this way is closely related to the experience and seniority of clinicians, and different doctors have different judgments on the same nodules. At present, there is no unified consensus on the diagnosis and treatment strategies of lung nodules recommended by multiple international consensus guidelines. In public health management facilities, the development and implementation of a comprehensive lung nodule lung cancer screening program is a complex and challenging task. Researching and proposing high-sensitivity and high-specificity, as well as simple, easy-to-popular and low-cost lung cancer screening technologies is an indispensable part of the healthcare system. In addition, due to the inconsistency of guidelines for the diagnosis and treatment strategies of lung nodules, the phenomenon of overdiagnosis and treatment of lung nodules is also common in clinical practice. How to avoid overdiagnosis and treatment needs more attention. Therefore, it is our responsibility to actively improve the accuracy of prediction of lung nodule canceration, reduce the rate of overdiagnosis and treatment, and increase the rate of early lung cancer intervention. Among the existing screening methods for early lung cancer, laboratory tests (especially the use of blood, urine or other liquid biopsies) are a low-cost, non-invasive and easily repeatable early prediction method compared with imaging or histopathological examinations, by detecting specific cancer biomarkers such as circulating tumor DNA, proteins, cancer metabolites, and even cell-derived exosomes and circulating tumor cells. However, there are still many challenges, including: 1) There are no effective and abundant tumor biomarkers for lung cancer; 2) There is no simple and feasible cancer detection method, especially in the asymptomatic stage; 3) There is no comprehensive analysis platform for large data sets to distinguish between healthy and lung cancer populations.

Raman spectroscopy (RS) is a non-invasive and highly specific material molecular detection technology that can be obtained at the molecular level to sensitively detect changes in biomolecules composed of proteins, nucleic acids, lipids and sugars related to tumor metabolism in biological samples. Surface-enhanced Raman spectroscopy (SERS) developed based on this technology is one of the feasible methods for highly sensitive biomolecular analysis technology. Although SERS technology has shown good diagnostic effects in a large number of preclinical studies of multiple tumors, it is limited by the generally small sample size and lack of external verification. Therefore, it is necessary to conduct clinical research on the use of Raman spectroscopy for tumor diagnosis, which meets the following requirements: 1. Objective, fast and practical Raman spectroscopy data processing methods are required, and machine and deep learning methods may be the best classification methods; 2. Multi-center, large-sample clinical samples are needed to train deep learning diagnostic models, and their true efficacy is verified by external data from prospective studies.

In previous study, the investigators collected serum Raman spectroscopy data from a cohort of 191 patients with pulmonary nodules, and built a Raman intelligent diagnosis system for benign and malignant pulmonary nodules based on a machine learning model. The accuracy of this intelligent diagnosis system reached 89.7%. In order to obtain the highest level of clinical evidence and truly achieve clinical transformation, this prospective, multi-center clinical study aims to verify the use of this intelligent diagnosis system for the early diagnosis of malignant pulmonary nodules.

Being tested
Serum Raman spectroscopy intelligent diagnostic system
Keywords
SERS, Raman, Early screening for lung cancer, Pulmonary nodule, diagnostic model
Medical subject headings
Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Serum Raman spectroscopy intelligent diagnostic systemDiagnostic test

    1. Screening interested participants should sign the appropriate informed consent (ICF) prior to completion any study procedures.
    2. The investigator will review symptoms, risk factors, and other non-invasive inclusion and exclusion criteria.
    3. The following is the general sequence of events during the 3 months evaluation period:
    4. Completion of baseline procedures Participants were assessed for 3 months and completed all safety monitoring.
Study groups in NCT06775587
Study groupRoleWhat they receive
Chest CT confirms patient with pulmonary nodulesChest CT confirmed the presence of pulmonary nodules in the patient and ultimately underwent surgical intervention. The pulmonary nodules had the final pathological results.
Receives: Diagnostic Test: Serum Raman spectroscopy intelligent diagnostic system

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Postoperative pathological results

    After undergoing surgical resection of pulmonary nodules, the final pathological nature of the pulmonary nodules was determined through pathological examination.

    Measured: through study completion, an average of 1 year

  2. Diagnostic accuracy

    Determine whether there is hematogenous metastasis in enrolled lung cancer patients through RAMAN intelligent diagnostic system

    Measured: through study completion, an average of 1 year

Secondary outcomes (2)
  1. Time to RAMAN diagnosis

    The time to perform RAMAN testing and obtain diagnostic results after obtaining serum

    Measured: up to 30 days

  2. Safety assessment Results

    AEs and SAEs through Day 30

    Measured: up to 30 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Jan 2025
  2. Study start8 Apr 2026 (estimated)
  3. Primary completion31 Dec 2026 (estimated)
  4. Study completion31 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
200 participants (estimated)
Target duration
1 Year
IDs, dates and publications
ClinicalTrials.gov ID
NCT06775587
Sponsor's protocol ID
2024-041
Acronym
SERS on lung
Status last verified
Mar 2025
First submitted
24 Dec 2024
Last updated
31 Mar 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Age, gender, smoking history, and tumor type of the enrolled patients

Questions about this trial

What is this clinical trial studying?

An observational study of Lung Cancer in Normal and Malignant Tumors, run by Fuzhou General Hospital at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 31 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Zongyang Yu, Ph.D (13509327806, yuzy527@sina.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Postoperative pathological results (time frame: through study completion, an average of 1 year). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Mar 2025.

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