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Status unknownNCT04215861Updated Jan 2, 2020

Clinical Study on Raman Spectra of Blood, Saliva and Urine in Patients With Cancer Treated by Modern Therapy

An observational study in Lung Cancer, Liver Cancer and Stomach Cancer, sponsored by The First Affiliated Hospital of Dalian Medical University. Status unknown at 1 site in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2020-01-02.

Sponsored by The First Affiliated Hospital of Dalian Medical University · Observational

The sponsor has not verified this record recently (last verified Dec 2019), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,000
Ages
18 Years to 80 Years
Sex
All
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Study summary

Blood, saliva and urine samples of tumor patients on the day of admission and discharge were collected for Raman spectral analysis, which provided exploration for the prediction of efficacy, follow-up and prognosis according to the variation characteristics of Raman spectral.

Read the detailed description

Blood, saliva and urine samples of tumor patients on the day of admission and discharge were collected for Raman spectral analysis, which provided exploration for the prediction of efficacy, follow-up and prognosis according to the variation characteristics of Raman spectral

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Conditions studied

  • Lung Cancer
  • Liver Cancer
  • Stomach Cancer
  • Breast Cancer

Browse trials for

03

In context

Stomach Neoplasms

2,851 studies on the registry are indexed under Stomach Neoplasms; 864 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 274 across 670 observational studies indexed under Stomach Neoplasms.

Browse Stomach Neoplasms studies →

Lead sponsor

The First Affiliated Hospital of Dalian Medical University is the lead sponsor of 41 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

  • 18-80 years old;
  • The patient whose tumor (tissue or cell) was first diagnosed by pathology;
  • Plan to receive routine clinical treatment: chemotherapy, radiotherapy, surgery, intervention, targeted therapy, traditional Chinese medicine treatment and biological immunotherapy;
  • Have relevant indications for treatment and have no contraindications;

Inclusion criteria

  • 18-80 years old;
  • The patient whose tumor (tissue or cell) was first diagnosed by pathology;
  • Plan to receive routine clinical treatment: chemotherapy, radiotherapy, surgery, intervention, targeted therapy, traditional Chinese medicine treatment and biological immunotherapy;
  • Have relevant indications for treatment and have no contraindications;

Exclusion criteria

Exclusion Criteria:

  • Severe or uncontrollable systemic diseases (such as unstable or uncompensated respiratory, heart, liver or kidney diseases, etc.);
  • Other circumstances considered inappropriate by the researcher to participate in the study;
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,000 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Raman spectra

    Blood, saliva and urine samples of tumor patients on the day of admission and discharge were collected to analyze the signal changes of Raman spectrum

    Time frame: the 1st day before operation

  2. Raman spectra

    Blood, saliva and urine samples of tumor patients on the day of admission and discharge were collected to analyze the signal changes of Raman spectrum

    Time frame: the 1st day after operation

Secondary outcomes

  1. progression-free survival

    Time frame: through study completion, an average of 1 year

  2. overall survival

    Time frame: through study completion, an average of 1 year

  3. objective response rate

    Time frame: through study completion, an average of 1 year

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Study locations

1 of 1 sites recruiting
  • The First Affiliated Hospital of Dalian Medical University
    Dalian, Liaoning 116000, China
    Recruiting
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 2, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04215861
Lead sponsor
The First Affiliated Hospital of Dalian Medical University
Responsible party
Sponsor
First posted
Jan 2, 2020
Start date
Oct 1, 2019
Primary completion
Oct 2021 (estimated)
Completion
Oct 2021 (estimated)
Last update
Jan 2, 2020

Study contacts

Xiaonan Cui, MD,PhD
Contact
cxn23@sina.com
+8618098876725
Xiaonan Cui, MD,PhD
principal investigator · The First Affiliated Hospital of Dalian Medical University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2019. You cannot join it, but the record below documents what was studied.

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