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The Clinical Study of Modern Therapies on Flora in Body Fluids and Blood of Malignant Tumor Patients

The Clinical Study of Modern Therapies on Flora in Body Fluids and Blood of Malignant Tumor Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04202848
Enrollment
500
Registered
2019-12-18
Start date
2019-12-20
Completion date
2022-11-11
Last updated
2019-12-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer, Gastrointestinal Cancer, Lung Cancer, Malignant Neoplasms

Keywords

Flora

Brief summary

The clinical study of modern therapies on flora changing in blood, oral cavity, urethra and intestinal tract of patients with malignant tumors. The study is observational. Patients are diagnosed cancer based on pathology or cell biology. The sample of flora will be obtained from their blood, oral cavity, urethra and intestinal tract, mainly to study what modern therapies lead to the influence of microecological environment including diversity and abundance of bacteria in patients who received malignant tumors. Immunological examination and Blood biochemistry evaluation include the number ratio, activity and function of immune cell, the immune cell marker(CD3, CD4, CD8, etc), C-reactive protein(CRP), tumor necrosis factor(TNF), Inflammatory stimulant factor(IL-2, IL-6, etc), tumor marker(CEA, AFP, etc),etc. Clinical evaluation includes image data(CT/MRI), quality of life(QOL), no disease progression survival, total survival, objective disease remission rate, etc.

Detailed description

This study collected samples of feces, urine, discarded blood and pharyngeal swab specimens from clinical laboratory from patients with malignant tumors in thoracic surgery department, general surgery department, oncology department and etc before and after treatments which contain chemotherapy, radiation therapy, immune targeted, endocrine therapy, surgery, traditional Chinese medicine and other modern therapies. Researchers will analyze the samples by oral flora, urethra, blood flora bacteria, the species diversity and abundance of the intestinal flora. Besides, quantitative analysis of inflammatory stimulators, c-reactive protein and tumor necrosis factor in peripheral blood was conducted to observe the relationship between the change characteristics of blood, oral, intestinal, urinary tract flora and urine composition caused by treatment and the therapeutic effect and prognosis.

Interventions

DIAGNOSTIC_TESTFlora analysis

diversity and abundance of bacteria in patients who received malignant tumors

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years

Inclusion criteria

1. Age 18-85 years old, male or female 2. Clinical diagnosis of malignant tumors 3. It is planned to receive cancer treatment 4. The genre of therapies is not limited, which contain chemotherapy, radiation therapy, immune targeted, endocrine therapy, surgery, traditional Chinese medicine and other modern therapies

Exclusion criteria

1. Cancer treatment before therapies 2. Previous history: He has suffered from intestinal microecology-related diseases such as cirrhosis, ulcerative colitis, Crohn's disease, irritable bowel syndrome, and urinary system diseases 3. Neurological, psychiatric or unconscious disorders. 4. The following drugs were used within 2 weeks before enrollment: 1. Probiotic preparations, various prebiotic preparations, etc 2. gastrointestinal peristaltic drug; 3. Take drugs known to have a significant effect on the intestinal and urethral flora within half a year (such as proton pump inhibitors, purgatives, bismuth, adsorbents, non-steroidal anti-inflammatory drugs, etc.) 5. Other situations that the researcher considers unsuitable to participate in the experiment;

Design outcomes

Primary

MeasureTime frame
The change of concentration of P-hydroxyphenylalanine metabolites in urinethe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of abundance of intestinal flora in faeces during therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of abundance of urethral flora in urine during therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of abundance of oral flora in pharyngeal swab in urine during therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of abundance of flora in blood during therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of concentration of purine metabolites in urine during therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of diversity of intestinal flora in faeces during therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of diversity of urethral flora in urine during therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of diversity of oral flora in pharyngeal swab during therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of diversity of flora in blood during therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months

Secondary

MeasureTime frame
The change of the number of immune cell marker(CD3, CD4, CD8, etc) in blood during the therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of the number of C-reactive protein(CRP) in blood during the therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of the number of tumor marker(CEA, AFP, etc) in blood during the therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of the number of Gastrin in blood during the therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months
The change of the number of tumor necrosis factor(TNF)-α in blood during the therapythe 1st day before the start of each kind of therapies, through cancer treatment, day 1, day 3, day 7 after treatment completion, 6 months

Countries

China

Contacts

Primary ContactXiaonan Cui, MD, PHD
cxn23@sina.com+8618098876725
Backup ContactYuwei Ma, MM
2932166904@qq.com+8618742567906

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026